Professional Documents
Culture Documents
Q-1(112)M&E/09
Q-1(114)M&E/09
:
CO2 laser sealed cavity RF-excited tankless
including surgical scanning fractional modes
Power
Average power
:
:
Transmission
Spot Size
:
:
Aiming Beam
Power Supply
phase
Cooling System
Standards
:
:
60 Watts
CW Mode: 0.05-60 Watts
Ultra Pulse Mode: 0.1 60 Watts
10.600 nm
2-225mJ (Adjustable)
Continuous, Repeat & Pulse mode
1-1000 Pulses/second (User selectable)
1ms-1sec
0.1 to 5.0 seconds
<2ms (Varies with pulse energy)
5-100%
Up to 2000 micro meter/pulse
:
CPG (Computer Pattern Generator) Gun
With seven shapes 2mmx2mm-10mmx10mm,
Micro Scanner, Micro manipulator
Articulated Arm, 360 degree rotation
1.3mm & 0.12mm
2000 micro meter, 1300 micro meter,
1000 micro meter, 200 micro meter,
120 micrometer.
Helium or Diode Laser
120V/200-240V, 20A/16A+10%, 50/60Hz, single
:
:
Wave length
:
Pulse Energy
:
Operative Mode
:
Repetition Rate
:
Time Range
:
Repeat Delay
:
Pulse Width
:
%Coverage/Pass
:
Depth of Penetration :
Scanner
Equipment must have 2 year comprehensive warranty &AMC for 5 years after expiry of
warranty.
Year wise rate of AMC to be quoted for 5 years. In case if firm is based outside
India , Indian agent for service should be located in Delhi/NCR. Preference will be given
to company with direct sales & service operations in India. There should be prompt after
sales service to reduce breakdown time to maximum of 2 days
Q-1(115)M&E/09
Laser
Wavelength
Frequency
: up to 10 Hz
Width of pulse
: 5-20 ns
Energy density
Spot diameter
: Variable 1- 8 mm
Cooling system
Delivery arm
Wattage
: 200-250 watt
Electrical requirement
: 210-230V/50Hz
Q-1(116)M&E/09
Q-1(117)M&E/09
2.
3.
4.
5.
Provision for cut mode, cut & coagulate mode, fulguration &
hemostasis mode.
6.
7.
7.
Bipolar pinpoint Microfine coagulation will be
preferable.
8.
8.
Q-1(118)M&E/09
IONTOPHORESIS MACHINES
- control system using fibre optics which allows the patient to
Q-1(119)M&E/09
WOODS LAMP
1.UV Light tube should emit 365 nm
2.main supply should be 230 volt AC
3.carrying case
4.Two ultra violet tubes are of 4 watts each
5.The unit should be compact portable
Q-1(120)M&E/09
Q-1(121)M&E/09
Q-1(122)M&E/09
Q-1(123)M&E/09
Q-1(124)M&E/09
HAND INSTRUMENTS
Trocar And Cannula, 11 mm, with manual valve control, trocar with
pyramidal tip. The cannula working shaft should be detachable from
the valve control body for better cleaning : Four
Trocar And Cannula, dia 5.5 mm, with manual valve control, trocar with
pyramidal tip. The working cannula should be detachable from the
valve control body for better cleaningTrocar : Four
Safety trocar with cannula, automatic valve, dia 11 mm: Two
Veress Needle, shaft length 150mm, dia 2 mm, with spring loaded and
leur lock connection: Two
Veress Needle, shaft length 120mm, dia 2 mm, with spring loaded and
leur lock connection: Two
HF cable for monopolar Instruments, 3 meters long: Four
Two way suction and irrigation cannula with trumpet valve, 5 mm & 10
mm
Q-1(125)M&E/09
Specification
Single Plate CR System with high resolution multi size dry imager
The CR System should be state of the art latest generation machine capable of handling
workloads of the hospital setup (No mobile models to quoted) It should have following
essential features along with CE/FDA approval.
1.
Imaging recording system ( Cassettes & Imaging Plates)
The following size of Radiology Cassettes along with Image Plates should be
supported by the unit. Image Plates must be Flexible to accommodate curved
cassettes in case of OPGs.
Sizes
Quantity
a)
14x17
4 Nos
2.
3.
4.
b)
14x17
4 Nos
c)
10x12
4 Nos
d)
8x10
4 Nos
e)
15x30cm
2 Nos
f)
18x24cm
2 Nos for mammography
Image Reading (Cr Reader / Digitizer)
a) The CR reader/Digitizer should be able to process up to 70 imaging plates/hour
or more, depending of size and application.
b) It should have a resolution of 5 or more pixels/mm (Minimum) for standard
resolution cassette and 10 pixels for high resolution cassettes reading.
c) The system should have option of having high resolution cassette/reading for all
cassette size including 14x17 & 14x14.
d) It should have a reading resolution of 20 pixels/ mm or more for
mammography.
Processing server/cr workstation with 19 LCD Panel.
a) PC based unified server/ workstation for centralized patient identification &
management of Images/ Studies.
b) Process of identification should be ready for interface with existing Hospital
information system (His) or Radiology information system (ris) in DICOM
protocols.
c) This server must provide display of acquired images with a greater details of
demographics, like patient/study listing for easy access.
d) This sever must provide full amount of post processing features like Geometric
corrections, Window/Level, Algorithms, Annotations such as markers,
predefined texts, drawing lines and geometrical shapes, Multi scale image
contrast amplification, measuring distances and angles and determining leg
length differences, shuttering, Histograms, Zoom, grey scale reversal, edge
enhancement, noise reduction, indicate grey scale saturation level, Latitude
reduction
e) This terminal must provide a full fledge DICOM printing, should be able to
print multiple formats (more than 4) of a patient study, print a true size.
f) Should be able to send DICOM images to a DICOM viewing station
g) Should be equipped with DICOM CD writer for allowing examination of a
patient to be written onto a CD in DICOM format for referral purposes.
Dedicated advanced work stations (4 Nos) other than console.
Should have 19 inch or more, antiglare, flicker free medical grade TFT/LCD flat
monitor with least one mega pixel resolution of standard make like BARCO.
a) Should have 320 GB or more storage capacity (hard disk), with 4 GB or more
RAM, latest high speed core 2 duo or any other processor of 3.0 GHz or more
speed and have CD & DVD Burner.
b) Should have latest window based original software.
c) It should have build in routine for using predefined image processing
parameters or image quality enhancement.
5.
6.
7.
8.
d) It should have mechanism for storing the patient image based on name, date,
exam, etc.
e) It should have capability of storing user defined image processing parameters
capability of overwriting predefined image parameter with user-defined
parameters & storing these two images separately.
f) It should be able to process the raw image date of CR reader and have capability
of window level adjustment, flipping, rotating, zooming, collimating,
annotating, latitude reduction, image noise reduction, grey scale saturation
feedback, electronic shuttering, grey scale reversal etc.
g) It should have provision for customized printing formats in different layouts.
h) It should have auto-routing incoming image to predefined DICOM store or print
destination.
i) It should have mechanism for printing multiple images in one film, with
possibility of slide and true size printing.
j) It should be able to connect with other DICOM system such as MR work
station, CT work station etc.
Laser / Dry Imager (for film printing)
a) The system must be a laser Dry imager, without need of any wet chemistry.
b) The system must be DICOM 3.0 print service class provider, allowing minimum
of 10 association at a time.
c) The system must be able to process up to 100 films/hour (minimum) depending
on the size.
d) The system must deliver its first film within 80 seconds from requested.
e) The system must have a spatial resolution of 500 PPI/DPI (minimum)
f) The system must have contrast resolution of 12 bits/pixel or more.
g) The system must have at three online film sizes, and should be capable to print
on any of the 8x10, 10x12, 11x14,14x14,14x17 sizes. All Three film
input trays should be freely configurable at user level for all the mentioned film
sizes.
h) The system must not involve any wet process and must give a dry film in singly
staged(without any users intervention) functionality.
i) The system must have a standard film sorter at the output for sorting the films
based on modalities connected.
j) It should have single step direct digital printing.
k) Required film for the imager should not be light sensitive.
Interconnectivity.
a) Interconnectivity between various CR modules should be Ethernet / TCp Ip
Based i.e. RJ 45 Connection ( 10/100 Base T/ Lan)
Connectivity to PACS
The system must be ready to integrate itself in PACS environment.
Software
a) Application related software like pediatric, black border/black masking should
be available.
b) The system should have software and hardware to perform full Leg-full
spine/Long Body Imaging /Image stiching.
9.
U.P.S
The company should provide UPS for the whole system with 10 Minutes backup.
10. Installation List.
Firm should attach installation list in India of the model quoted out of which at leat
Installation should be in Govt Hospital or Govt. Medical institute.
11. The equipment should have comprehensive guarantee for five years for all parts
including electronic parts & CR Plates.
12. For should give unconditional under taking for 98% uptime warrantee and acceptance
of increasing the guarantee period by double the down time if it is in excess of 2%.
No cap on the period of extension will be accepted.
13. CMC for next five years also to be quoted for the complete system for which order
will be placed with unconditional under taking for 98% uptime warrantee and
acceptance of increasing the guarantee period by double the down time if it is in
excess of 2%. No cap on the period of extension will be accepted.
14. Firm should have service center in Delhi/NCR. Firm to provide no and names of
services engineers them Delhi/NCR.
Original Data sheet of technical specification of the equipment quoted to be provided
along with point wise compliance statement mentioning deviation if any with
justification. The original data sheet should indicate reference to technical
specification point wise by highlighting ink.
Q-1(126)M&E/09
4.
5.
6.
7.
8.
9.
Q-1(128)M&E/09
1. The processor should be capable of processing the maximum film size 14x17 and
minimum film size 4x4. It should be able to process all types of x-rays & Imaging
films including ultrasound films, Mammography & CT Scan films.
2. It should give completely dry film after processing.
3. The output obtained from the processor should be at least 75films per hour of size
14x17 in 90 second mode.
4. There should be provision for automatic replenishment of developer and Fixer.
5. Developing Tank should be minimum of 5 liters, Fixing tank should be minimum of 5
liters and washing tank should also be minimum 5 liters capacity for prolonged
processing and should have replenishment container of 25 Liters.
6. Developer and fixer replacement should have automatic program with appropriate tank
capacity. Replenishment time should be adjustable between 20-90 seconds with
possibility of turn off.
7. The container assembly should be mono shell and made of material, which is noncorrosive and of latest technology.
8. The functions should be microprocessor controlled.
9. It should be automatic control with thermostat for developer and fixer. The temperature
should have automatic control with thermostat and the temperature should have a range
of 280c 360c.
10. The processing time should be variable between 1.5minute to 3.0minute in steps of not
more than 8 seconds for perfect fine tuning of contrast.
11. Dryer temperature should have automatic control of temperature.
12. The processor should go into stand by mode if not in use for long time and the stand by
mode should be attained in less than 1 minutes.
13. It should have and auto-fill program facility for developer and fixer bath.
14. Processing time, Temperature and replenishment rate should be adjustable from the
control panel itself.
15. It should have digital display of temperature and timing for developer bath, process time,
Error message and film time indication etc.
16. It should have water saving mode, anti-crystallization and anti-oxidation mode.
17. Transport speed should be adjustable form the control panel and should be
microprocessor controlled.
18. There should be at least two micro-sensors fro film detection and also separate level
sensors for Developer & Water tanks for overflow protection.
19. Multiple program memory should be there for different application. At least two program
memories must be there.
20. The processor should be complete with the following operational electrical data- 230
volts, 50 Hz, Single Phase. The firm should provide and appropriate Voltage servo
controlled stabilizer of Rating not less than 3 KVA.
21. AMC should be furnished for 5 years after expiry of warranty period for whole system.
22. Any plumbing work required for installation shall be done by the firm without any extra
cost.
23. The equipment should have comprehensive guarantee for five years for all parts including
electronic parts.
24. Firm should give unconditional under taking for 98% uptime warrantee and acceptance of
increasing the guarantee period by double the down time if it is in excess of 2%. No cap
on the period of extension will be accepted.
25. Firm should have service center in Delhi/NCR. Firm to provide no and names of services
engineers located them Delhi/NCR.
26. Original Data sheet of technical specification of the equipment quoted to be provide
along with point wise compliance statement mentioning deviation if any with
justification. The original data sheet should indicate reference to technical specification
point wise by highlighting ink.
Q-1(129)M&E/09
Kidney bridge
10. Measurements:
Height: 730-1230 mm
Trendelenburg: 25 to 35 degree
Offers for models that are more advanced and have advantages over the model
having the above features will also be considered.
The measurements given above are approximate and minor variations without
alteration of function are acceptable. List of installations in major institutions in
Delhi must be quoted.
Q-1(130)M&E/09
19. The warranty clause should be clearly specified with optional provision for extended
warranty
20. The accessories should include trolley, mains cable, foot switches for mono and
bipolar, reusable and single use neutral electrode for adults and children, cable for neutral
electrode, fixing belt for neutral electrode (chi Id/adult), securing buttons for fixing belt,
sterilisable and or disposable electrode handle with and without finger switch, cable for
electrode handle, set of electrodes (long and short), electrode container with holder, tip
cleaner, bipolar forceps, cable for bipolar forceps, cable for connecting to mono polar and
bipolar laparoscopic instruments and vessel sealing system for open and laparoscopioc
surgeries.
21. The rates for all the accessories should be quoted individually and separately
22. Terms and conditions of after sales service contract. both comprehensive and
otherwise, ten years after warranty period should be quoted
23. Facility for after sales service should be available in Delhi
24. Manufacturer's undertaking to provide after sales service for ten years
period after warranty either directly or through the authorized agent should be submitted
25. Set should be available for demonstration if required.
Offers for models that are more advanced and have advantages over the model
having the above features will also be considered.
The specifications given above are approximate and minor variations without
alteration of function are acceptable. List of installations in other major
institutions in Delhi must be quoted.
Q-1(131)M&E/09
Offers for models that are more advanced and have advantages over the model
having the above features will also be considered.
The specifications given above are approximate and minor variations without alteration
of function are acceptable. List of installations in other major institutions in Delhi must
be quoted.
Q-1(132)M&E/09
Instrument
Reusable Veress
Pneumo- peritoneum
Needle
Reusable Trocar :11mm
Reusable Trocar :5mm
Specifications
spring loaded blunt stylet luer lock
length 10cm
multifunctional valve, insufflation
stopcock and threaded sleeves,
pyramidal tip, length (10.5cm)
multifunctional valve, insufflation
stopcock and threaded sleeves,
pyramidal tip, length (10.5cm)
Quantity
12
4
8
13
14
15
16
Knot pushers
Needle holder coaxial
type
17
4
5
6
10
11
12
18
6
6
4
2
3
4
1
19
20
Hassan cone
Reduction sleeve
2
4
21
Fascia closure
instrument
Offers for models and instruments that are more advanced and have advantages
over the model having the above features will also be considered.
The specifications given above are approximate and minor variations without
alteration of function are acceptable. List of supplies in major institutions in Delhi
must be quoted.
Q-1(133)M&E/09
7. Luminous intensity in the light field should be 270 or more lumens per watt
8. Illuminated field diameter should be:
Min: 140 - 200 mm
Max: 250 - 350 mm
9. Depth of illumination should be 90-120 cm or more
10. Special filters to filter out 99.9% of infrared component of the emitted light so that
there is increase in intensity of light without increase in heat
11. Temperature increase in operating field should not be greater than 2- 4 degree C
12. Temperature of light head should be specified.
13. The light head should be so constructed as to provide optimum conditions for laminar
flow
14. Colour rendering index should be 92-98. Should provide optimum colour temperature
which is close to color temperature of day light.
15. Light field adjustment by sterilisable handle.
16. Control panels on the light assembly as well as away from it for adjustment of light
intensity, illuminated area and on/OT controls
17. The system should have features which make it simple to clean and disinfect and
maintain
18. Service lamp life should be more than 15,000 -18,000 hr's for LED light and 1000
1500 hrs for halogen bulb and 4000 5000 hrs for Xenon bulbs.
19. Easily replaceable system components.
20. Terms and conditions of after sales service contract both comprehensive and
otherwise, ten years after warranty period should be quoted
21. Facility for after sales service should be available in Delhi
22. Manufacturer's undertaking to provide after sales service for ten years
period after warranty either directly or through the authorized agent should be submitted
23. Set should be available for demonstration if required.
Offers for models that are more advanced and have advantages over the model
having the above features will also be considered.
The specifications given above are approximate and minor variations without
alteration of function are acceptable. List of installations in other major
institutions in Delhi must be quoted.
Q-1(135)M&E/09
-do-
do-
F) Cystoscope- urethroscope sheath 16 F; length 22 cms with obturator & two luer
lock adapters; Instrument channel 1 X 5 Fr or 2X 4 Fr.
G) Cystoscope- urethroscope sheath 14 F size with obturator; Instrument channel 5
Fr X 1.
3. A) Telescopic bridge with 1 lockable instrument channel for adult sheath.
B) Same as above for pediatric sheath.
4.) OPTICAL BIOPSY FORCEPS
A) Adult size- fitting adult sheath-double action jaws.
B) Optical grasping forceps-double action jaws.
C) Marberger sen. Optical short jaw Bx forceps double- action jaws- for use with
Hopkins II, 30 degree telescope.
=20 in no.
=10 in no.
= 10 in no.
4 Environmental factors
1. Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General Requirements
of Safety for Electromagnetic Compatibility or should comply with 89/366/EEC; EMCdirective.
2. The unit shall be capable of being stored continuously in ambient temperature
of 0 -50 deg C and relative humidity of 15-90%
3. The unit shall be capable of operating continuously in ambient temperature of
10 -40deg C and relative humidity of 15-90%
5 Power Supply
1. Power input to be 220-240VAC, 50Hz fitted with Indian plug
2. UPS of suitable rating with voltage regulation and spike protection for 120
Q-1(137)M&E/09
8.
9.
Direction of view
Depth of field
Field of view
Outer diameter
Instrument channel
Working length
Range of distal end bending
Forward
3-100 mm (approx.)
1300 or more
9.0 mm or more
3.2 mm or more
1.0 1.30 meters
Up 1800 or more
Down 900 or more
Right & left 1200 or more
1.
2.
3.
4.
Direction of view
Depth of field
Field of view
Outer diameter
Forward
3-100 mm (approx.)
1300 or more
12 mm -14 mm
5.
6.
7.
Instrument channel
Working length
Range of distal end bending
8.
9.
3.2 mm or more
1.30 1.70 meters
Up & down 1800
Right & left 1600 to 1800
10.
Others
AMC
A)
B)
2.
3.
Firm should give an undertaking that the spare parts will be made
available for three years after the expiry of warranty period.
Firm should under take to enter into AMC (for periodic / preventive as
well as break down call on site) for three years after the warranty period.
Warranty : Minimum 3 years
Up-gradation facility
Q-1(138)M&E/09
2.
3.
It should be able to record the ECG at the speeds of 25 and 50 mm per second.
4.
Should be light weight (less than 3 kg) and portable & have system for 1mV
Calibration.
5.
6.
7.
Should have rechargeable built in battery, with battery discharge and battery
charging indicator.
8.
9.
Should have AC, muscle and anti-drift filters & safety standard class I CF
type.
10.
11.
12.
13.
Warranty for 2 yrs & AMC for minimum 5 yrs after expiring of warranty.
14.
Q-1(139)M&E/09
Q-1(140)M&E/09
A.
B.
Individual SpecificationsI.
II.
III.
Autoclavable PCR Eppendorf racks for the following volumes 0.2ml, 0.5ml and 1.5ml (pack of 500) - 4 Units each.
IX.
X.
XI.
Q-1(141)M&E/09
Q-1(142)M&E/09
GENERAL-
MAGNIFICATION
40X-1500X
OPTICAL SYSTEM
EYEPIECE TUBE
EYEPIECE LENS
OBJECTIVES
COARSE/FINE FOCUSING
STAGE
LARGE
STAGE
WITH
SUPER
HARD
COATED
RECTANGULAR SURFACE STAGE. 74-80 X 50-56 MM
CROSS TRAVEL RANGE USING LOW POSITIONED
COAXIAL X AND Y MOTION CONTROL ON RIGHTHAND
SIDE
CONDENSER
FLUORESCENT ATTACHMENT
ILLUMINATION
DIGITAL CAMERA
2 YEARS.
THE AGENT MUST BE STATIONED IN DELHI
COMPREHENSIVE MAINTENANCE
CONTRACT5 YEARS AFTER WARRANTY PERIOD.
SPARES -
Q-1(143)M&E/09
MICROSCOPE BODY
1. Motorized Zoom Magnification system with apochromatic optics
2. Magnification 2.1X to 21.5 or better activated by hand grip and foot control with manual
override
3. Eye piece 12.5X
4. Internal Motorized fine focusing system, activated by hand grip and foot control
continuously
5. Adjustable working distance from 200 mm to 500 mm or more without exchange of
objective lens, manual override, integrated continuously variable illumination field spot
size
6. integrated beam splitter with two additional output inbuilt for connection of coobservation device and video
7. Stereo co observation system for assistant surgeon/ teaching purpose
Future up gradation to XY module
BINOCULAR TUBE
1. 180 Degree or more tilt able binocular tube with focal length f= 180 mm or more
2. Graduated knob for continuous adjustment of inter- papillary distance from 55 mm to 75
mm.
EYE PIECE
1. Pair of wide field push in eye piece 12.5 X with magnetic locks
2. Diopter setting from -8 D to +5 D
ILLUMINATION SYSTEM
1. Coaxial xenon illumination minimum 180 Watt with a back up lamp changer Xenon or
halogen bulb
HANDGRIPS
1. Easily removable handgrips with adjustable keys for zoom and focus
2. Four freely programmable keys for setting illumination intensity, controlling the
video camera
Cont..2
Page-2
FOOT CONTROL PANEL
1. Control keys for zoom, focus, movements and light intensity
-- 20 numbers
Q-1(144)M&E/09
INSTRUMENT
QUANTITY
Operating laryngoscope
Adult size-18cm- Large
Operating laryngoscope
Adult size-18cm-Medium
1
1
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
1
1
1
3
1
1
2
2
2
2
2
1
2
1
1
3
2
1
1
2
2
1
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
Q-1(145)M&E/09
2
1
1
1
1
3
2
2
1
1
2
2
1
1
1
1
3
3
2
2
1
1
Q-1(146)M&E/09
2.
3.
4.
5.
6.
7.
Q-1(147)M&E/09
Q-1(148)M&E/09
SPECIFICATIONS FOR INTRA-OPERATIVE FACIAL NERVE MONITERING SYSTEM
A microprocessor controlled system for recording the motor nerve responses during surgery is
required.
The system should work on 220V/50Hz mains only and have the following specifications:
MAIN UNIT:
EMG Channels
Noise
Bandwidth
Audio Output
STIMULATOR:
:
:
:
:
Minimum 2 Nos.
< 10 mV P/P( Peak- Peak)
10 Hz - 10 kHz
14 W
:
:
3Hz or 30 Hz selectable
50uA- 5 Ma
Q-1(149)M&E/09
Q-1(150)M&E/09
MICROSCOPE
1.
2.
3.
4.
5.
RIGID ENDOSCOPES
1.
2.
3.
4.
5.
6.
1.
2.
3.
4.
5.
6.
7.
Q-1(151)M&E/09
Q-1(152)M&E/09
B. TECHNICAL SPECIFICATIONS:
a) Cabinet should be made of Sheet steel corrosion resistant with cover with
interlook.
b) Swing-out and fixed angle rotors with adaptors as well as microplate rotors
should be available.
c) Maximum speed should be of approx 5000 rpm with Swing out / 18000 rpm with
angle.
d) Maximum RCF should be 3885 g swing out/235000 g angle.
e) Maximum capacity should be for 4 x 100 ml Swing-out / 12 x 1.5/ 2 ml Angle
f) Temperature range should be between -10C and + 40C
g) The control panel should have Start/Stop switch, Stop less speed regulator, Zero
start switch, Continuous ready digital- technometer.
h) It should have Automatic timer and cut off, Digital speed meter, unbalance switch
and dynamic braking.
i) The Digital displays should show Program No., Speed, RCF, & Time.
j) It should have at least 10 program memories.
k) It should have timer at 1-99 minutes and hold position.
l) It should have at least 5 acceleration and 5 braking rates.
m) It should have maintenance free induction drive.
n) Automatic rotor identification system with overspeed protection.
o) The system should have totally CFC free refrigerant fluid and insulation
p) The system should have Angle Rotor of
200/400/500 l
q) The system should have Angle Rotor: 30x15ml for glass tube with adaptors for
different size.
r) Swing-out Rotor: 4 places with bucket with max speed 5000 rpm and max rcf
13,500g. Lid for bucket and adaptors for different sizes should be available.
s) The system should include all accessories required to centrifuge 28 15 ml glass
tube or more tubes.
t) The system should have a guarantee of at least 2 years followed by AMC for 5
years.
uploading from the insulin pump and continuous glucose monitoring system (real time).
Q-1(154)M&E/09
Q-1(155)M&E/09
Q-1(156)M&E/09
Q-1(157)M&E/09
Q-1(158)M&E/09
Q-1(159)M&E/09
Q-1(160)M&E/09
Q-1(161)M&E/09
Q-1(162)M&E/09
Research Camera
Software:
Q-1(163)M&E/09
Specifications
Technical data:
Construction details
Outer chamber
Inner chamber
Shelves
Elements
Temperature control
Ventilation
Control Panel
Q-1(164)M&E/09
Outer chamber
Inside Dimension
Shelves
Heating elements
Thermometer
Control Panel
Ventilation
Q-1(165)M&E/09
DEPARTMENT OF MICROBIOLOGY
Technical specification for Laboratory Centrifuge
1.
2.
3.
4.
5.
6.
Q-1(166)M&E/09
Q-1(167)M&E/09
Q-1(168)M&E/09
1.
2.
3.
Built in fan
4.
5.
Adjustable shelves
6.
7.
8.
9.
+ 5oC
Q-1(169)M&E/09
MICROPIPETTES (Imported)
1.
2.
3.
Single channel
4.
Autoclavable
5.
Light weight
6.
7.
8.
9.
10
Volumes
Micro centrifuge
Specifications:
-
Q-1(171)M&E/09
Q-1(172)M&E/09
MAGNIFICATION
EYEPIECE TUBE
EYEPIECE
NONSEPIECE
STAGE
STAGE SIZE
OBJECTIVES
OBJECTIVE
N.A
W.D
30.0MM
7.0MM
0.65MM
0.23MM
CONDENSER
ILLUMINATION SYSTEM
COARSE/FINE FOCUSING
Q-1(173)M&E/09
Q-1(174)M&E/09
Q-1(176)M&E/09
Q-1(178)M&E/09
The system should have Installation at reputed sites with proven track record
in the field.
The parent company must have Head quarters based in India.
The company should be well represented with service engineers and
application support team based in New Delhi.
Q-1(179)M&E/09
Specifications
1.
2.
3.
4.
Q-1(180)M&E/09
Specifications
1. Female Pelvic model of flexible synthetic bone-like material with dismantable pelvic
floor.
2. Shows details of pelvic floor.
3. The model shows external genitalia and associated muscles.
Q-1(181)M&E/09
BLOCK CABINET
(SPECIFICATIONS)
1. Allows for the organized storage of blocks that have been embedded using: Tissue
Cassettes,
Biopsy
Cassettes,
Mesh
Cassettes,
Mega
Cassettes,
Processing/Embedding Cassettes and Embedding Rings
2. One-piece construction eliminates hinges and doors for dust-free storage.
3. Six impact-resistant plastic drawers feature generous space for identification.
4. Compact in size and stackable.
Q-1(182)M&E/09
SLIDE CABINET
(SPECIFICATIONS)
1. Allows for the convenient storage and retrieval of microscope slides or transparencies.
2. Two different vertical filing drawer sections can be stacked in any combination.
3.
Each 1" drawer section has 11-16 drawers and holds 400-500 slides per drawer.
Q-1(183)M&E/09
1.
Temperature:
-20 to-25
2.
Door:
3.
4.
Alarm:
Adjustable alarm system with automatic audible
and visual warnings for overtemperature, undertemperature,
power failure, low battery, and system maintenance provide
immediate status of critical functions.
Lockable
5.
Shelves:
6-9
6.
7.
8.
Internal Illumination
9.
Frost free
10.
11.
12.
Q-1(184)M&E/09
(SPECIFICATIONS)
(Mini PAGE+ Transfer Apparatus)
Q-1(185)M&E/09
Specifications
1.
2.
Q-1(186)M&E/09
Specifications
1. Capacity:- Six Bodies
2. Temperature:- +2 0 C to +8 0 C
3. Outer Panels: - Outer is made of stainless steel of Galvanized sheet of thickness & grade
finished with bacteria resistant coating.
4. Interior: - Durable Stainless steel interiors to give better life and makes cleaning easy
providing hygienic conditions and great sturdiness.
5. Insulation: - Safe, high density, non-setting & Thick polyurethane insulation of 80 to
100mm.
6. Doors: - Standard hinged door with easy grip handle & standard key block.
7. Floor & Frame: Recessed Floor & superior engineered frame.
8. Racks & Trays: Sturdy SS rack system with railings for easy movement of SS trays with
castors constructed heavy duty use.
9. Refrigeration:- Strong and reliable with powerful quick response refrigeration which runs
on demand, and exclusive long life SPENCERS superior refrigeration process in an
unique feature of SPENCERS Mortuary freezers. Salient features include: Heavy duty
Air-cooled compressor. Highly efficient air cooled finned condenser with automatic
condensate evaporating system. Internal evaporator system. Internal evaporator system.
Non-CFC/non-HCFC environmental friendly based on compressor capacity. Forced air
circulation maintains chamber uniformity.
10. Temperature Control: The unit is fitted with a digital electronic temperature controller
cum indicator for easy readability along with audible alarm system. The electronic
management system allows to set the temperature as required as per the standard
temperature range of the Mortuary cabinet.
11. Alarms: In built high & low temperature alarms are usually incorporated in all the models
of SPENCERS Mortuary Freezers.
12. Temperature chart recorder.
13. Humidity controls.
Q-1(187)M&E/09
Q-1(188)M&E/09
Name of Equipment: Data Acquisition System with accessories and Analysis software
1.) Data Acquisition System (Strictly to the following Specifications only)
SNo
Feature
Specification
a)
Input Channels
MUST HAVE Eight (8) analog input channels
including eight (8) single ended inputs through BNC
connectors and choice of four (4) DIFFERENTIAL
inputs
b)
Differential Input Supply Voltage
MUST HAVE + 5V Regulated for direct connection of
Powered Transducers
c)
Sampling Speed
d)
e)
f)
Amplification range
g)
Data Communication
h)
i)
Expansion Ports
j)
Quantity
Specification
a)
Channels
b)
Exporting Data
c)
Display Modes
d)
Online Computations
e)
Specialized Analysis
FREE UPGRADES
g)
GLP
h)
Quantity
Feature
Technology
b)
c)
d)
e)
Application
Measurement unit
Animal Model
Flow probes
f)
Calibration
g)
Interface
h)
Quantity
Application
Frequency response
Signal Artifacts
Model
Calibration
Interface
h)
i)
Sensor size
Quantity
Specification
MUST BE based on Ultrasound transit-time
technology the Gold Standard
Real-time Cardiac Output
ml/min
Rats and rabbits
1) For vessel diameter - 1.5-2.0 mm
2) For vessel diameter - 1.8-2.5 mm
MUST allow software Calibration using above
software.
Should connect to the Input (BNC) of the Data
Acquisition system.
Flowmeter - 1
Flow Probes 1 Each
Specification
MUST BE based on Mikro-tip Technology the Gold
Standard
Recording Intravascular and Ventricular pressure
Up to 10Hz
NO Motion Artifacts or Signal Attenuation
Rats and rabbits
MUST be supplied with calibration kit
MUST be able to connect to above Data Acquisition
system through a signal amplifier.
3F Side-mounted
1
Name
Amplifer for Biopotentials with Needle
electrodes
Specification
Amplifier
Input amplifier: High impedance, differential
(floating), electrically isolated
Quantity: 1
Amplifier
Input configuration: Differential
Amplification range: 200 V to 5 V full scale in 14
steps
Low-pass filtering: 1 Hz to 2 kHz in eight steps
(software selectable)
Frequency response (-3 dB): 2 kHz maximum at all
gains with the 2 kHz filter selected.
Quantity 2
Fluid-filled Pressure Transducer
Operating pressure range: 20 to 300 mmHg
Maximum excitation: 15 V DC or AC
Sensitivity: 5 V/V/mmHg
Operating temperature range: +10 C to +50 C
7.)
Quantity 2
Amplifier
Max Range: +1 Inches H2O
Amplification ranges: +20 mV to +500 mV full scale
in 5 steps
Max Input Pressure:+28.1 Inches H2O(7kPa)
Low-pass Filtering: 1, 10 and 100 Hz (software
selectable) using fourth order Bessel filter.
Quantity: 1
Flow Heads
Flow Rate: + 10 L/min (Rabbit) + 1 L/min (Rat)
Dead Space Volume: ~2mL (Rabbit) ~0.6mL (Rat)
Flow at 10 mmH2O: 12L/min (Rabbit) 1.2L/min (Rat)
8.)
Quantity: 1 Each
Signal Conditioner
Operating Principle: Non-invasive blood oxygen
saturation (SpO2)
Saturation range: 70 100%
Measurement rate: 1 reading per second
Quantity: 1
Sensor
Based on patented Nonin SpO2 technology
9.)
Ventilator
Quantity: 1
Suitable small Animal ventilator
10.)
Quantity: 1
Compatible Computer, Printer and UPS.
Quantity: 1
Q-1(189)M&E/09
Name of Equipment: Telemetry system with analysis software
Telemetry System
ONLY Data Acquisition system (At least 16 Channels General purpose inputs) based Telemetry system for
lifetime monitoring (24/7) of freely moving lab animals and recharging in situ ONLY (No specialized
servicing/factory replacement of battery).
1.) Data Acquisition System (Strictly to the following Specifications only)
SNo
Feature
Specification
k)
Input Channels
MUST HAVE Sixteen (16) analog input channels
including sixteen (16) single ended inputs through
BNC connectors and choice of four (4)
DIFFERENTIAL inputs
l)
Differential Input Supply Voltage
MUST HAVE + 5V regulated voltage for direct
connection of Powered Transducers
m)
Sampling Speed
MUST HAVE aggregate sampling speed of 400,000
samples per second.
n)
Variable Sampling Speed on Every
It is mandatory to have VARIABLE SAMPLING
channel
SPEED on every channel.
o)
ADC Resolution
Should have at least 16 bit resolution
p)
Amplification range
q)
Data Communication
r)
s)
Expansion Ports
t)
Quantity
Specification
i)
Channels
j)
Exporting Data
k)
Display Modes
l)
Online Computations
at Events
m)
Specialized Analysis
n)
FREE UPGRADES
o)
GLP
p)
Quantity
Feature
Signals
2
3
4
Sampling Frequency
Transmission
Animal size
Specification
Should be able to record 3 signals simultaneously:
Pressure, Temperature and (low and high frequency) biopotential.
Up to 8000 Hz
Digital transmission on multiple transmission bands
Rats (>200g) and larger
5
6
7
8
9
10
11
Recording range
Monitor duration
Continuous data
Schedule Data
Refurbishment
Co-housing/co-implants
Output format
12
Quantity
Up to 5m
UNLIMITED- should recharge in situ
True 24/7 (For small animals)
Remote switch at receiver or via software
No Refurbishment of waiting, recharge and continue recording.
High frequency data from multiple animals
Standard analog voltage and MUST allow acquisition with supplied
Data Acquisition system.
1
Transmitter power-down in situ, via the receiver, to conserve and extend battery life
Transmitter battery is easily recharged using Power Supplier; therefore no battery refurbishment is
required.
Feature
Pressure accuracy
Pressure drift target
Frequency response
Pressure range
Ambient pressure range
Maximum operating altitude
Temperature operating range
Transmission range
Transmitted signal
Channel
11.
12.
Outer material
Transmitter on-off mechanism
13.
Scheduled acquisition
Specification
1 mmHg
< 2 mmHg per month
DC to 150 Hz (-3 dB)
-20 to 300 mmHg
650 to 800 mmHg
1300 m
8 to 41 degrees Celsius
Up to 5 m
Digital in the 2.4 GHz band
12 transmission frequencies are available to
support multiple transmitters in one area
Medical grade silicone elastomer
Remote control via the receiver, manually or under
software control
Hardware supports full remote automated
14.
Calibration
2.
3.
Heating Plate
4.
Specification
A switching device that allows recording, using
Data Acquisition system and software, of up to 8
Telemetry transmitters with a single receiver.
The Scheduler switches the receiver to record from
multiple individual transmitters through a single
input. The device is controlled using the supplied
software. It should allow data recording durations
and periods to be specified allowing a system to
record from hours to days from multiple telemetry
transmitters.
Quantity: 1
Surgical instruments and components required to
implant arterial transmitters in rats.
1x 0.5 ml gel for re-gelling pressure catheters, 1x 3
ml bottle of tissue adhesive, surgical training DVD,
4x catheter introducers, 8x suture tabs, 1x 2 m 4-0
suture material and needle. 2x Halsted-mosquito
hemostats (12.5 cm), 1 x no. 5 fine straight forceps,
1 x no. 5 curved fine forceps, 1x Adson forceps 12
cm, 1x Wullstein Retractor 4.5 cm spread, swabs,
swab sticks and absorbent surgical spears.
Quantity: 1
Temperature feedback control for controlling small
animal (rats) temperature through a heating plate.
Accuracy: 0.5C, Resolution: 0.1C, Range:-100
to +400C.
Heating Plate size: 111 mm x 217 mm.
Quantity: 1
Compatible Computer, Printer and UPS.
Quantity: 1
Q-1(190)M&E/09
Description: 1.
2.
3.
4.
Q-1(191)M&E/09
Description: Should enable measurement, computation, printout of all Spirometry, Flow Volume
Parameters, Maximum Ventilation Volume, Inspiratory Capacity, Expiratory
Reserve Volume, etc.
System should have Dry Rolling Seal Spirometer (12 Litre Capacity).
Range
Accuracy
:
:
Volume 0 to 12 Litres.
Volume 2%; Low 3%.
Should incorporate less than 0.06 cms H2O/Lsec, for highest accuracy &
reproducibility
Should have in built graded scale for calibration procedure (0-12litres).
Accuracy of measurement should not be effective with Relative Humidity, water &
Saliva droplet.
Should be supplied with USB interface for computer, Operating window Software,
Standard accessories & instructions Manual.
Computer Pentium IV 3.0 GHz or more CPU, 512 RAM, 15 VGA Colour Monitor, CD R/W
Drive, Keyboard, Mouse, Window 2000, Hard Disc Drive (1 80 Gbyte), HP DeskJet Printer, to
be supplied.
Q-1(193)M&E/09
LYOPHYLYSER (Imported)
1
2
3
4
5
6
7
Condenser capacity
Final temperature in condenser
Number of compressors
Nominal vacuum pump flow
Voltage (single Phase)
Warranty
Post Warranty AMC
Q-1(194)M&E/09
Wavelength range
400750 nm
Photometric
Photometric range
0.03.5 OD
Bandwidth
10 nm
Linearity
Accuracy
Reproducibility
Resolution
0.001 OD
Light source
10
Photodetectors
11
Filters
12
Read time
13
Plate shaking
14
Plate types
15
Warm-up time
3 min
16
Interchannel variation
17
18
Data output
Onboard graphical thermal printer and USB2 interface with PC or Mac data
stations
19
Data storage
20
Multilanguage support
21
Dimensions (W x D x H)
22
Weight
Microplate washer
24
25
26
27
28
29
30
Microplate Washer should include bottle and tubing set, port manifold, aerosol protection cover
Microplate Washer should be compact programmable 8-channel manifold microplate washer /
aspirator, with buit-in vacuum and dispensing pumps designed for use with 96 well plate and strip
plates, with flat bottom, U,V-shaped wells.
It should have aerosol protection of the working area; the removable plate carrier is auto-clavable for
easy disinfection. The system should be programmable, with a large choice of washing methods
It should have a wide choice of wash sequences to facilitate protocol creation and storage, and is
Compatible with 96-well microplates that have flat-, U-, or V-bottom wells and strips.
It should have accuracy of 0.1mm for bottom washing, crosswise aspiration, and overflow washing.
The washer should have plate-shaking option to help minimize bubbles and adherence of liquid to
well sides
The washer has waste bottle sensor to detect high waste liquid levels
31
32
The Washer should have programmable washing sequences for customized protocols
It should have integrated vacuum and dispensing pumps to ensure accurate and quiet washing and
to eliminate the need for external pumps
33
34
Warranty: 2 Years
Post Warranty AMC: 5 Years
Q-1(195)M&E/09
Test Method
5
6
Number of Standards
(Multipoint cal)
Quality control
User programmable
8
9
10
Photometer Lamp
Photometric Linearity
Wavelengths
11
Reagent Blank
Memory
Flow Cell/Manual
cuvett position
Aspiration System
12
13
14
15
16
17
18
19
2 Years
5 Years
Q-1(196)M&E/09
Sensitivity
2.
7.
Minimum
sample volume
Photometric
principle
Light source
Monochromator
Measuring
wavelength
range (on both
EX and EM)
Bandpass
8.
Resolution
3.
4.
5.
6.
S/N 800 or better (RMS), using Raman band of water, S/N 250 or
better(Peak to Peak), Excitation wavelength 350nm, bandpass
5nm, response2s.
0.6ml
Monochromatic light monitoring ratio calculation
150W xenon lamp, self-deozonating lamp house.
Stigmatic concave diffraction grating: 900 lines/mm
200 to 750nm (expandable up to 900nm with optional detector)
Wavelength
accuracy
10 Wavelength
scan speed
11 Wavelength
drive speed
12 Response
1nm
30,60,240,1,200,2,400,12,000, 30,000, 60,000nm/min
60,000nm/min
Response from 0 to 98%
13 Photometric
-9999 to 9999
Value range
14 Data processing PC: Windows* XP Professional
Unit
15 Printer
Printer compatible with Windows*XP
16 Provision of Polarization accessory for UV/VIs. (Wavelength range 260-700nm.
17 Provision of Micro plate accessory for automatic measurement using a 96 will micro
plate
18 Incorporates flexible software features such as quantilation analysis function,
wavelength scan measurement, time based measurement, Data export function for
excel, print previews etc.
19 Two sets of extra cuvvetts each of Quartz and Glass may also be provided
20 Warranty
Two years
21 Post warranty
Five years
AMC
Q-1(197)M&E/09
7- It should be capable of Optimizing, saving, and quickly recalling the imaging acquisition
settings.
8- Should have motorized zoom lens- f/1.2, 12-75mm with numerical feedback.
9- Safe DNA Imaging without UV exposure- using the XcitaBlue Conversion screen to
prevent damage from UV and preserve samples for downstream protein production.
10- Reproducibly position or center the sample on the image platen by using gel alignment
templates.
11- Should have live image acquisition records real time development of the
chemiluminescent reaction. thus removing the guesswork often involved with single
event film capture of blot signals.
12- Should come with 1 D analysis software with following features
A- Automatic band & lane detection, Mol wt & purity analysis.
B- VNTR applications, Phylogenetic tree & dendogram.
C- Should have automation manager.
D- Should have a multichannel viewer to overlay multiplexed or
multifluorescent samples.
13- Atleast 2 sets of reagent kits should be provided with the equipment.
14- Warranty : 2 Years
Post Warranty AMC : 5 Years
Q-1(198)M&E/09
Q-1(199)M&E/09
40X -1000X.
OPTICAL SYSTEM
OBSERVATION TOBE
EYEPIECE
NOSEPIECE
OBJECTIVE
Plan Achromat objective. 4X, 10X, 20X, 40X, 60X, & 100X.
FOCUSING SYSTEM
STAGE
ILLUMINATION
PHOTO SWITCH
CONDENSER
OTHERS
3-5 mega pixel *IEEE 139a Fire wire interface with adapter and
Application Software.
The Microscope should be upgradable to Fluorescence (Six position turret), Phase contrast, DIC and
Multi teaching attachment up to ten head.
5 years Warranty
Q-1(201)M&E/09
Hb variants
B Thalassemia testing
Total Glycated Hemoglobin
Hemoglobin A1c
Hb A2
HbF
Hemocystine
Catecholamines in Urine and Plasma
VMA
Serotonin
Anti Epileptic Drugs
Anti Depressants Drug
Vitamin B1, B2, B6
System Specifications
- control
- Max. Operating Pressure
- Flow Accuracy
+/- 1.0% or 30 ul/min whichever is
greater
- No. of Eluents
One or two
- Programmable flow rate
0.000-10.000ml/min, increments,
standard 100 uL headsCom
- Operating temp. Range
Normally 4o C to 40oC
Can vary for dedicated software,
(test wise)
- Operating Pressure Limits Dedicated Software Programmable
High & low Pressure Limits
- Inject Switch
control Closure, Pre-wised
- Flow During Switching
Continuous
- Loop Fill
Partial or Full
- Loop Size
Changeable, ul 5 mL
Complete with: Gradiant Pump, Detectors, Integrator Computer, Printer and Dedicated columns
and one each kit of above tests.
If closed System Rate quotation of kits for next five years.
- Installation and demonstration at place of working.
- Working manual
- 5 yrs warranty
- Start up reagents for 1000 tests.
- Standard accessories, spares as per catalogues.
- Should have authorized dealer /service centre in Delhi.
- Equipments should be complete in all aspect to start working
from day one including
printing of results.
- Quotation for all consumables.
Q-1(202)M&E/09
FLOW CYTOMETER
A Bench Top Cytometer operable at 220V, 50 Hz is required with following specification:
1.
Should be equipped with 488 mm Solid State Diote laser with at least 20m W or more power output at the
high quality quartz flow cell.
2.
The equipment must be able to perform at least five fluorescence parameters along with Forward and Side
Scatter simultaneously.
3.
Optical filters should be easily changeable by user without having to call service engineers.
4.
The equipment should have approx. 20 bit or more data processing with 4 or more decade of data display.
5.
The equipment should have sample loading option of automated Multi Carousel tube loading of at least 24
tubes more along with 96 multi- well plate loading. It should also have biohazard contained wash station for
thorough rinsing of sample probe.
6.
Must have provision for both real-time and List mode (Off-line) full compensation so as to obviate the need
for repeat sample runs.
7.
The equipment should have an integrated bar-code reader to define the tube & plate holder position to ensure
true positive sample identification.
8.
9.
Software: PC controller Windows based software preferably latest version. Software should display and
control instrument processes.
10. Hardware with following configuration or better: Pentium Core 2 Duo Processor, RAM 4 GB, Graphics Card,
Hard Drive 160GB, Network ports, DVD with Read-Write Devices, 8 USB ports, 22 Flat Monitor & UPS of
appropriate electrical specifications.
11. The company should submit manufactures original product catalogue with specification details.
12. The bidder may be asked to demonstrate the equipment if required by purchaser.
13. Starter up kit including sheath fluid, calibration kits, cleaning solution and sample tubes to perform 2000
assays.
14. The fluorochromes workable on the system should be able to do a wide range of diverse applications for
Cancer Research and Clinical Investigations.
15. Compatable on line UPS.
16. 5 years comprehensive warranty.
Q-1(203)M&E/09
Cancer Surgery
Q-1(204)M&E/09
Abdominal retractors
Balfour retractor Baby
Balfour retractor child size-lateral blades 58mm center blade 45x
80mm
Denis browne retractor small frame
Quantity
1
1
1
Self-retaining retractors
Jansen Retractor 4x4 prongs-Blunt
Weislander retractor 2x3 prongs Blunt-105mm
Weislander retractor 3x4 prongs Blunt-165mm
Adson-Baby Retractor 4x3 Prongs Blunt
Finichietto infantBlades 19x21mm
Finichietto child Blades 45x36mm
Finichietto medium blades 65x45mm
1
1
1
1
3
2
1
Retractors
Parker Langenbeck retractor
Langenbeck Blades 25x 6
Langenbeck Blades 25x 6
Czerney Retractor
Doyens Retractor
Morris Retractor
Jolls thyroid retractor
Deavers retractor-adult
Deavers retractor-Child
Desmarres set of four
Allison wire lung retractor child
Malleable retarctors set with assorted sizes
Haemostatic forceps
Halsted Mosquito 125mm straight
Halsted Mosquito 125mm Curved
Criles Forceps 140 mm straight
4
4
4
4
2
4
1
2
2
2
2
2
12
20
12
20
6
6
6
6
3
3
2
6
6
6
6
6
4
1
Dissecting forceps
Dissecting forceps150 mm Plain
Dissecting forceps150 mm toothed
Dissecting forceps200 mm Plain
Dissecting forceps200 mm Toothed
Adson Forceps 150 mm plain
Adson Forceps 150 mm toothed
Micro Adson Forceps 150 mm toothed
Adson Forceps 180 mm plain
Adson Forceps 180 mm toothed
De Bakey dissecting forceps 2mm Jaws 150mm
De Bakey dissecting forceps 2mm Jaws 200mm
De Bakey dissecting forceps- angled 2mm Jaws 150mm
De Bakey dissecting forceps- angled 2mm Jaws 200mm
Russian dissecting forceps 180mm
Russian dissecting forceps 200mm
Tuttle dissecting forceps 200mm
Tuttle dissecting forceps 230mm
Denis browne Grasping forceps 180mm
McGills forceps--small
McGills forceps--medium
8
8
6
6
4
4
4
4
4
4
4
2
2
6
6
6
6
6
2
2
Scissors
Iris Straight 115mm
Iris Curved 115mm
Metzenbaum straight 150mm
Metzenbaum straight 200mm
Metzenbaum curved 150mm
Metzenbaum curved 200mm
Reynaulds curved 150mm
Reynaulds curved 200mm
0
Potts190 mm 45
Baby Metzenbaum straight 145mm (Tungsten Carbide)
Baby Metzenbaum Curved 145mm (Tungsten Carbide)
6
6
8
8
8
6
6
6
2
3
3
Needle Holders
Mayo Hegars 150mm
Mayo Hegars 200mm
Mayo Hegars 230mm
Debakey 180mm
Debakey 200mm
Debakey 230mm
Ryder 150mm (Tungsten Carbide)
Ryder 180mm (Tungsten Carbide)
Ryder 200mm (Tungsten Carbide)
8
8
6
6
6
6
3
3
3
6
6
6
2
3
1
1
Miscellaneous
Clip applying forceps 200mm
2
2
2
1
2
1
1
2
2
1
1
2
2
2
2
2
2
3
20
Focusing system:
Working distance:
2. BINOCULAR TUBE:
Binocular tube:
180-degree tiltable
Focal length of 190 mm or better
Interpupillary distance: adjustable of from 50 mm to 80 mm
Equipment For Face-To-Face Surgery: (For all Microscopes)
Stereo bridge(integrated beam splitter) with two additional output ports for
connection of coobservation device and videocamera,
180-degree tiltable binocular tube with focal length of 170 mm,
Pair of push-in eyepieces 12.5x with magnetic lock,
Pair of rotatable adapters +/- 22.5 degrees Stereo Coobservation system with
two joints for assistant surgeon/teaching purpose
3. EYEPIECES:
Widefield, >12x with magnetic locks,
Diopter setting from 8D to +5D, also suitable for spectacles wearers
4. ILLUMINATION SYSTEM :
Coaxial xenon illumination
Quick-action lamp changer
Back-up xenon lamp
Must provide two additional Xenon bulbs
5. HANDCONTROL PANEL:
Detachable
For zoom and focus, illumination intensity and video camera control
6. FOOT CONTROL PANEL:
For zoom and focus, XY movements, light intensity
7. FLOOR STAND: Rollable with magnetic Brakes
Brake control with hand control
8. LCD DISPLAY: Set up of different parameters
Activation at press of a button
A)Equipmentmusthave2yearscomprehensivewarranty&AMCfor5yearsafter
expiryofwarranty
B)YearwiserateofAMCtobequotedfor5years.Incaseiffirmisbasedoutside
India,IndianAgentforserviceshouldbelocatedinDelhi/NCR.Preferencewillbe
giventocompanywithdirectsales&serviceoperationsinIndia.Thereshouldbe
promptaftersalesservicetoreducebreakdowntimetomaximumofTwodays.
Q-1(206)M&E/09
Q-1(207)M&E/09
Should be made by Mild Steel material, treated with Zinc phosphate and Epoxy Powder
Coated.
Should have dimension of L 2150 X WI1000 X H440 -660 mm
Should have bed frame size approx 2000 mm X 915 mm
Should have Weight approx 85 Kgs
Should have castor dia of 125 mm swivel with diagonal brake
Should have backrest 750, footrest 450, Hi-Lo-elevation operated by hand crank.
Should have ventilated 4- panel mattress base
Should have removable ABS moulded head and food board, with Maica lamination.
Should have collapsible epoxy- finish safety side rails with spring loaded lock.
Should have 2 1V pole mount & 4 pole mount attachment at, at all corners of bed frame.
Should have roller bumpers at all corners to protect body frame
Should be supplied complete with 100 mm PU foam mattress with Nylex covering.
Should be quoted with 2 years warranty and 5 years AMC charges
Q-1(208)M&E/09
5
6
7
8
9
10
11
12.
13.
14.
15.
16.
17.
18.
19.
20.
21.
22.
23.
24.
Made of powder-coated die cast aluminum, with smooth and clean surfaces that
are easy and safely to clean.
Dust and splash proof.
One point suspended, diameter above 500mm.
Light system:
Surgical Light should have cold and shadow free light, High Light intensity
Very homogeneous large area and in depth illumination of the Surgical field
Multi- lens matrix technology.
The intensity should be adjustable.
Light field should be adjustable from 20cm to 30cm and focusing via sterilizable
handle in the center of the light head.
Switching the light head on and of should be possible in sterile or non sterile
Manner directly at the light head as well as on the LCD wall control panel. From
One single control LCD panel, either only the respective light head or the
Complete light combination must be able to switch on and of simultaneously.
No heat emission through IR radiation.
High fail- safety through optical light system consisting of between 70 to 200 LEDs, with
its own lens. In case of failure of one light source (LED), the illumination of the light field
is not affected. Even in case of failure of a second or more light sources, negative effects
on the illumination of the surgical fields remain limited to a minimum.
Aerodynamic designed dome of the light head should support the effect of laminar air flow
systems.
There should be a Sterilizable knob at the lower side of the light head to control of all light
intensity and other functions should be also be controllable from control centre i.e. diming,
endo- light , intensity , shadow control, switching on/off and camera zoom by the surgical
team itself .
Lighting intensity at 1m distance: 160,000 Lux
Size of light field at 1m distance: 18-28 cm
Colour temperature: 4000k-5500k
Colour rendering index: RA95 to RA97.
R9 (deep Saturated red color index) : 95 to 96.
Life span of main light source : 20,000 hours 30,000 hrs
Supply Voltage : 110 240 VAC/24V DC/24 VAC
A suitable disposable camera cover with integral clear lens should be provided which
allows surgical team to grasp camera module to aim camera or adjust the pattern size or
intensity of light.
Camera should not need independent power connection and should draw power from light
head only.
Monitor Arm:
25.
The lighting system should have a third arm with digital display monitor of 19.
26.
The monitor arm should be pre-wired with compper/multimode fiber optic cable bundle
with Video enab led system to support various Customer-defined Video options.
The Shadow less light should have integrated high resolution camera system with sealed
camera optics to save it dust and fluids.
The show less Operating Light should have a powerful single chip camera having optical
zoom lens for Video Photography as per the following specifications.
The cameras should have features like digital signal processing and digital zoom lens.
The camera should have a digital memory mode to capture digital images directly into the
DVD recorder for easy transfer to DVD disc:
Single Chip : type CCD images sensor
Standard : PAL/NTSC
Pixels : approx above 300,000 pixels resolution
Zoom : 40 x optical zoom ration, (10 x optical, 4x digital)
Focal lens distance : = 10mm (wide angle) to 1000mm (telescopic)
Signal/Noise ratio : exceeds 49 dB
While balance : Automatic/Manually (with auto focus)
Recorder
32.
33.
34.
DVD recorder of reputed make with attached LCD display of at least 17 for viewing the
recording after the operation is over.
The recorder should be either kept in the OT room on shelf or should be remotely
mountable in another site with network cabling.
LED Surgical Lighting system should meet applicable standards such as FDA
UL;EN/CE/CSA etc.
Q-1(209)M&E/09
a.
(Control Unit
Digital Display for Transmission/Reduction Ratio of the Hand Piece and Pump
Output.
Visual Indication for Sense of Rotation of the Motor.
Maximum Pumping Capacity: 100 ml/min.
b.
(Micro Motor)
c.
f.
g.
h
i
1 No
(Foot Switch)
(Motor Cable)
1 No.
1 No
(Support Plate)
1 No
Support Plate Complete with Swivel-Bar and Fixation Device for Motor and
Accessories.
Support Device for Bottle .
1 No.
Pump Tubing Autoclavalbe, Silicone
1 Pair
Spare Tubing Autoclavalbe, Silicone 1 M, Diameter 1 mm for Connection to
Hand Piece.
1 No
Plug- 1n Mandrel for Bottle Ltr.
1 No
System should be equipped with A Solid Roller Pump for Supply of Cooling Water.
Clockwise / anti clock rotation
Control Unit is provided with a Memory Circuit
Finally adjusted values are relevant and can be perceived on the Display in next
operation .
1 No
III
a.
1 No
1 No
IV
a.
Micro Oscillating Saw without Saw Blade, Integrated Irrigation Tube with Fork Wrench,
Recommended Maximum Speed 15.000 rpm.
1 No
Saw Blade with Short Shank, Working Length 11mm, Thickness of Blade 0.3 mm Blade
Length 14mm, size 6mm, 10mm & 15mm Total Length 27mm.
5 each
Saw Blade with Long Shank, Working Length 26mm, Thickness of Blade 0.3 mm Blade
Length 14mm, size 6mm, 10mm & 15mm Total Length 42mm.
5 each
VI
Micro Sagittal Saw without Saw Blade Integrated Irrigation Tube with Fork Wrench,
Recommended Maximum Speed 20.00 rpm.
1 No
Saw Blade for Micro Satittal Saw Thickness of Blade 0.35 mm, Size : 10x 4mm, 10
x6mm, 15 x 6mm ,15x10mm, 27x12mm.
12 each
Micro Osseoscalpel Saw with Blades
a.
Oseoscalpel Micro Saw with Axial/Sagittal Cut, Oscillating Hub, Especially suitable
for three Dimensional cutting
b.
Saw Blades for Osseo scalpel Micro Saw, Thickness of Blade 0.35mm , Working Length
12 mm, 18 mm &24mm.
12 each
VII
Mucotome
a.
Steinhauser Thickness of Cut 0.2-1.2mm, width of Cut 22 mm Max Maximum Speed
rpm 5000.
b.
c.
5pkt
d.
VII
1 No.
1Pc
b
Screw Holding, Device with 2-Pc Fixation Clamps, 1-Pc Retaining Spring and 1
Screwdriver 1set
c
Pc
d
Pc
e
Pc
f
Pc
g
Pc
Insert for Slotted Screws with Central Ping Guidance with Screws Head 3.0mm
1 Pc
Insert for Slotted Screws with Central Ping Guidance with Screws Head 2.5mm
1 Pc
j
Pc
Insert for Screws with Tampered Inside Hexagon with Screws Head 4.0mm
IX
Tools
2 each
2 Nos
c
each
Diamond dust Abrasives Style Bud 44mm long, Dia 4.50 & 7.00 mm
Trephines 44mm Long, Dia 1.80, 2.30, 2.70, 5.00 & 7.0mm
2 each
2 each
HSS Twist Drills 44mm Long Dia 0.50, 0.60, 1.00,1.20,1.50, 2.10 & 2.30
5 each
2 each
h
each
Hough Crurotomy Burrs, Serrated Cutting 65mm Long, Dia 1.0,1.20 & 2.70mm
2 Nos
2 each
k
each
a.
1 No
2 Nos
pieces.
D
XI
10 PCs
b.
50 PCs
1
Should quote complete set with Original catalogue
2
Should carry a warranty of two years and AMC of five Years
3
Price of accessories /blades/burrs etc should be quoted separately. The quantity may vary
as per requirement.
Q-1(210)M&E/09
TECHNICAL SPECIFICATION
ULTRASOUND THERAPY UNIT
The unit must have the following specifications:
Ultrasound frequencies
1 and 3 MHz
Intensity:i)
ii)
Pulsed :
Continuous
0-3 W/cm sq
0-2 W/cm sq
Display
Intensity in W/cm.sq
Timer
65%
Treatment head
Main Supply
Battery Charger
Safety class
TUV/GS
Q-1(211)M&E/09
06
06
06
06
12
12,
06
24
24
Wire cutter
Should have following specification
DI.N 1.4021x20 Cr13:
With the components 0.17% C and 13% Cr
Guarantee of 5 years
18 cm, 7 for 1.5 mm wire
22 cm , 10.5 for 3mm wire
04
04
23 cm 9
04
Osteotome
Should have following specification
DI.N 1.4021x20 Cr13:
With the components 0.17% C and 13% Cr
Guarantee of 5 years.
18 cm 7 6mm
18 cm 7 8mm
18 cm 7 10mm
22 cm 8 10mm
22 cm 8 15mm
22 cm 8 20mm
04
04
04
04
04
04
Chisel
Should have following specification
DI.N 1.4021x20 Cr13:
With the components 0.17% C and 13% Cr
Guarantee of 5 years.
16 cm 6 4mm
16 cm 6 6mm
16 cm 6 8mm
16 cm 6 10mm
13.5cm 5 4mm
13.5cm 5 6mm
13.5cm 5 8mm
04
04
04
04
04
04
04
CRANIOFACIAL INSTRUMENT.
1 set (200
2
2
2
2
2
2
2
Q-1(212)M&E/09
SPECIFICATIONOFHYDROSURGERYSYSTEMFORBURNSLOUGHREMOVAL
Equipmentshouldbesuitableforuseinburnpatients
Shouldbeoperableon220VA.C.electricity.
Shouldconsistofpressuregeneratingconsoleandhandpiecewithfootswitch
control.
Consoleshouldgenerateenoughhydrostaticpressuretoformwaterjettoseparate
sloughfromburnsurfacebylocalizedvacuum(Venturieffect)atendofhand
piece.
Handpieceshouldcombinglavageandaspirationofremovedtissue
simultaneously.
Shouldhavedifferenttypesofhandpieces.30handpiecesmustbeprovidedwith
theequipment.
Shouldcarryaguaranteeof2years&AMCfor5years
Pricesofhandpiecesshouldalsobequotedseparately.
Q-1(213)M&E/09
INTERFERENTIALTHERAPYUNIT
Twochannelinterferentialelectrotherapyunit
Shouldhavelargedigitalparameterdisplay
Theunitshouldhave2and4poleIFT.
TheunitshouldhaveTENScurrentasymmetrical.
TheunitshouldhaveTENSwithcurrentburst.
Theunitshouldhavepreprogrammedtreatmentprotocols.
Thetreatmentprotocolsshouldbeadjustableandrewriteableforflexibilityin
use.
Shouldhavefacilityoffixingpersonalizedstartupprogrammetosavetime.
TheunitshouldcarrytheInternationalSafetyStandard.
Q-1(214)M&E/09
SPECIFICATIONFORBINOCULARLOUPEFORPLASTICSURGERY.
Q-1(215)M&E/09
Q-1(216)M&E/09
12 Nos
12 Nos
12 Nos
6 Nos
15 Nos
15 Nos
C. Microvascular clamps
Micro clamps should be light , compact robust corrosion resistant & have unique gripping surface
. They should have smooth sliding bar action on all approximator clamps for vessel diameter of
0.4mm to 5.0mm, pressure of 5 gm/mm2 to 15gm/ mm2. Should have size and type (artery or
vein) marking on them.
I. Single Microvascular clamp for Artery (1A):
12 Nos
12 Nos
12 Nos
12 Nos
12 Nos
12 Nos
12 Nos
12 Nos
12 Nos
12 Nos
12 Nos
12 Nos
D. Microvascular Neddleholders
Needle holder should be specially designed for secure grip due to parallel closure over the entire
jaw length and closing pressure precisely calibrated for minimising fatigue. Should be strong and
fine
I. Needle Holder:
15cm long, Round handle, Curved
II. Needle Holder
18cm long, Round handle, Curved
12 Nos
12 nos
E.
Vessel dilator
should have special ball point form of the tips so that the dilating pressure is evenly distributed
over the entire area of the vessel.
I. Vessel Dilator
12 Nos
11cm long, flat handle 9 mm wide, angulated 10 degree, dia 0.20
II. Vessel Dilators
12 Nos
11cm long, flat handle 9 mm wide, aungulated 10 degree dia 0.30
E. Clamp applying forceps15 cm long:
6 nos
6 nos
6 Nos
H. Clamp box:
6 Nos
A)Equipmentmusthave2yearscomprehensivewarranty&AMCfor5yearsafter
expiryofwarranty.
B)YearwiserateofAMCtobequotedfor5years.Incaseiffirmisbased
outsideIndia,IndianAgentforserviceshouldbelocatedinDelhi/NCR.Preferencewill
begiventocompanywithdirectsales&serviceoperationsinIndia.Thereshouldbe
promptaftersalesservicetoreducebreakdowntimetomaximumofTwodays.
Q-1(217)M&E/09
Emergency
DDD
80ppm
DOO
80ppmor current setting.
Mode
Rate
Output Amplitude
10 mA
10 mA
20 mA
25 mA
Atrial
Ventricular
Pulse width
1.0 ms
1.5 ms
1.0 ms
1.5 ms
Atrial
Ventricular
Sensitivity
0.5 mV
2.0 mV
asynchnous
asynchnous
*
*
*
Atrial
Ventricular
A-V Interval
Sensed
Paced
PVARP
Upper Rate
Rapid Atrial pacing rate
140 ms
170 ms
300 ms
110 ppm
320 ppm
1.
2.
3.
4.
5.
6.
7.
.
*
9 volt battery
Product literature/manual(details)
Disposable pouch
Ventricular patient cable
Atrial patient cable
Heart wire receptacle seals
Carrying case
: 10 nos.
: 1pc
: 1 pc.
: 10 pcs
: 10 pcs
: 10 pcs
: 1 pc
Q-1(218)M&E/09
1.
Description of function
1.1
2.
Operational requirements
2.1
4)
5)
2.2
1.
2.
3.
-23.1
5-Pump Console
1. The unit should have 5-pump console compactly arranged with separate power
supply and control modules. Should have easy access connectors for
interchanging the pump.
2 Each individual roller pump should be capable of running independently on
180-270 V/50-60 Hz supply.
3 Should have a spill proof base.
The unit should be supplied with a Battery backup for at least two pumps, all
safety systems and accessories for a minium of 60 minutes. Switch over from
main power to battery backup should be automatic and immediate. The
battery unit should be built in to the pump base and it should be recharged
automatically when the system is operating with main power supply.
4. Individual pump heads should have Harvey Roller pumps with facility for tubing to be
used adjustable from to 5/8 through 3/8 and by easily changeable mechanism
5. Individual pump heads should have display in digital- The total infusion volume in
litres and delivery time, the flow rates in LPM and in RPM.
6. Each pump should have easy mechanism for occlusion setting for different thickness of
tubes available in the market 1/32 to 3/32
7. Should have unidirectional hand crank facility as a critical safety feature hand crank
loading should be from top for faster access.
8. The Console should have a compact base mount for the entire pump heads together,
with pole and handles.
9. Should have variable,changeable tubing holders in each pump head:1/4,3/8,1/2,5/8
and double
10. Should have movable oxygenator holder.
11. Roller pump should have a self diagnostic circuit with provision to detect and display
critical alarm conditions. Optional Pulsatile module which can be monted on any of the
blood pump.
3.2 Should have a venous control module with single pole mast with electronic
venous line occluder.
3.3 Should have a monitor mount with adjustable monitoring arm
3.4 Instrument tray positionable with ling monitoring arm
3.5 Lightweight surface table,writing surface
-33.6
3.7
MONITORS:
PRESSURE MONITOR: Facility to monitor one arterial line pressure and one
cardioplegia line pressures (toatal2);along with necessary pressure transducer, cables
six(2X3) and domes reusable, with accurate digital display and alarm facilities audio
and visual.
TIME MONITOR: 6 temperature displays for patient monitoring and for cardioplegia
monitoring with digital display in Celsius with 6 necessary compatible temperature 6
probes and 6 additional probes(6X2=12 probes) with 3X2=6 of them for nasal, rectal
and esphageal use
-4-
5.
5.1
5.2
5.3
3.8
AIR-OXYGEN BLENDER:
To work at 50-60 PSI for membrane oxygenator with water trap attached with necessary
hoses and connections of minimum of 5 meters length and with triple flow glass flow
meters.
3.9
SAFETY DEVICES: Safety monitor should have optional capability for computer
interface to retrieve perfusion data
ULTRASONIC AIR SENSOR:Ultrasonic air sensor to detect bubbles to work equally
well with crystalloid and blood,should be possible to fit anywhere in the circuit easily.
LEVEL SENSOR SYSTEM: Ultrasonic transducers to work well with crystalloid and
blood with adhesive pads, with alarm settings.
3.10
ASSESSORIES
1. STAINLESS STEEL LINE CLAMPS for cardio pulmonary bypass 12 Nos.
2. REMOTE CONTROL MODULE FOR THE TEMPERATURE CONTROL
MONITOR:
Optional remote control unit should be capable of taking 9 Temp. Probes
and display temperature in digital readouts. Alarm limits setting for at least
three probes at crucial sites.
3. INSTRUMENT TRAY WITH MOUNTING ARM
4. AT LEAST ONE THERMAL BALNKET
5. ON LINE MEASUREMENT OF PH,PCO2 @ HB FOR NEONATAL
CARDIAC SURGERY
4.
4.1
4.2
4.3
4.4
4.5
4.6
6.
6.1
6.2
6.3
Power Supply
Power input to be 180-270VAC,50-60Hz/440 V 3 phase as appropriate fitted with special
imported plug dedicated to the unit.
Resettable over current breaker shall be fitted for protection
Suitable UPS of with voltage regulation and spike protection for 60 minutes back up
7.
7.1
7.2
7.3
7.4
8.
8.1
8.2
8.3
Documentation
User manual in English
Service manual in English
List of important spare parts and accessories with their part number and costing available in
stock with the supplier.
Certificate of Calibration and inspection from factory.
Log book with instruction for daily, weekly, monthly and quarterly maintenance checklist.
The job description of the hospital technician and company service engineer should be
clearly speltout.
List of Equipments available for providing calibration and routine Preventive Maintenance
Support as per manufacturer documentation in service/technical manual.
8.4
8.5
8.6
9.
10.
11.
Q-1(219)M&E/09
40 KV to 125 KV
up to 125 mAs
4 ms to 2.5 Sec
Rotating Anode with 0.8X0.8 mm focal spot
Auto shut off collimator with Halogen 100 Watt
Integrated with collimator
9.Cassette Box:
Storage 8 Cassettes
10.Unit should operate on single phase, 15 Amp plug on 200-240 volt A.C without any
external transformer
11.Quoted unit should have AERB/BARAC Certificate
12.The equipment should have comprehensive guarantee for five years for all parts including
electronic parts and X-ray tube
13 Firm should give unconditional under taking for 98% uptime warrantee and acceptance of
increasing the guarantee period by double the down time it is in
excess of 2% No cap on the period of extension will be accepted.
14 Firm should have service center in Delhi/NCR Firm to provide no and names of services
engineers located them Delhi/NCR
15 Original Data sheet of technical specification of the equipment quoted to be provided along
with point wise compliance statement mentioning deviation if any
with justification. The original data sheet should indicate reference
to technical specification point wise by highlighting ink.
16 Demonstration is a must
Q-1(220)M&E/09
hours or the company will provide the replacement of same or higher configuration
equipment.
14. Demonstration is a must.
Q-1(221)M&E/09
Description of Function
1.1
1.2
2.
Operational Requirements
2.1
3.
Technical Specifications
3.1
Pneumatics:
Drive System: Stepper motor driven bellows
Drive gas-helium(Available with disposable canister or refillable cylinder.
Pumping Volume: 0.5cc-50cc Counter pulsation rate: 40-200 pulsations per minute
In Automatic Mode: System should be capable of automatically selecting
appropriate trigger i.e. ECG or Pressure and also accurately select the inflation
and deflation points, in automatic mode. In automatic mode of operation user
should be in control of the deflation point. In Automatic mode Advance software
should automatically adapt the timings for various rhythms and rate variations,
without any user intervention. In Automatic mode it should automatically
identify Arrhythmias and adopt R wave deflation mode for better patient support,
without any user intervention In Manual mode the system allows user control of
most of the pump functions.
Should be able to trigger on 7 mm Hg of Pulse pressure when used in Pressure Trigger
mode
Single key start-up to make it fast, user friendly and easy to use
Should be able to display at least 3 wave forms as ECG, Invasive Pressure and Balloon
Pressure wave form & Pace maker spikes if paced.
Large display for brighter and very good visibility from a distance in lighting conditions
3.2
3.3
3.4
3.5
3.6
3.7
3.8
3.9
3.10
3.11
3.12
3.13
3.14
3.15
3.16
3.17
3.18
3.19
3.20
3.21
4.
4.1
4.2
4.3
On screen indication for Helium level in the cylinder and battery level for timely
intervention and correction.
ECG inflation marker to indicate inflation period on ECG which can be useful when
arterial pressure form is not available.
On screen indication of standby time and should give alarm after 15-30 minutes, to draw
users attention on the system being on standby
System should be approved for use on Pediatric patients and Pediatric balloons should be
supplied with the system
-2IABP to function without any disturbance, when cautery is used on patient; when on ECG
trigger mode.
Optical Blood leak detect for early indication of blood coming into the balloon lumen due
to IABP leak
Should have extensive Help Text available during startup to make the system easy to use
even for new users.
Should give extensive Help messages to correct the alarm conditions that are specific to the
alarm condition. This should help the user to overcome the alarm problems immediately
and with ease.
Should be capable of removing condensation automatically without user intervention and
should be maintenance free.
Should have Peripheral Vascular Doppler for detecting limb ischemia, which is attached to
the main equipment
Should have automatic Altitude correction to make it safer for the use during Air Transport
Should have software which allows the user to monitor the IABP from any remote location
via a modem
In-built Comprehensive Service Diagnostics to help the technician to locate the fault
immediately
Should have capability to connect on the Hospital network
Integrated Printer OR Chart recorder to print the reports
System Cinfiguation Accessories, spares and consumables
System as specifiedSystem should be supplied with the following:
ECG cable with Refillable Helium cylinder Compatible with the IABP system Qty:3 Nos
Intra Aortic Balloon Catheter for Adults, Size: 40cc Qty:2 Nos
Intra Aortic Balloon Catheter for Adults, Size: 30cc Qty:2 Nos
Reusable Invasive Blood pressure transducer system with pressure flush device system.Qty: 2
Nos
5.
5.1
Environmental factors
Shall meet IEC-606001-1-2:2001(Or Equivalent BIS) General Requirements of
Safety for Electromagnetic Compatibility. Or should comply with
89/366/EEC;EMC directive.
5.2
The unit shall be capable of being stored continuously in ambient temperature of 0-40 deg
C and relative humidity
5.3
The unit shall be capable of operating continuously in ambient temperature of 10-40 degC
and relative humidity of 1-90%
6.
Power Supply
Power input to be 170-270 V AC,50Hz fitted with Indian plug
On line UPS of suitable rating with voltage regulation and spike protection for 60 minutes back up
-3-
Q-1(222)M&E/09
Weight (base unit without vaporizers or cylinders) i.e. Trolley Mount (cart) 115 kg (250 lbs.) appx
Dimensions of Trolley Mount (cart) 80cm x 135 cm x 75 cm
Power supply 100 - 240 VAC, 50/60 Hz., 2.5 A max.
Battery (supports both ventilator and monitor) 45 minutes
Technical DatMONITOR
The standard system consisting of a CPU base unit with a separate SVGA monitor, compatible with any
standard Multi-synch display.
I) Comprehensive Integrated parameter set includes dual V-lead ECG,SpO2, respiration, temperature,
cardiac output, invasive and non-invasive blood pressure
II) Easy to learn and use Automatic configuration of parameter boxes, simple menu structure,
sync output, RS 232, and remote keypad, alarm output, video output, R 50 recorder,
PCMCIA
Analog output
Signals: ECG, arterial blood pressure
Delay: < 25 ms
Mechanical Specifications
Size
H x W x D: 100 mm x 368 mm x 368 mm
(4 x 14.5 x 14.5 in)
Weight 19 lbs (8.5 kg)
Information Management Capabilities
Data storage: 24 hours of trended parameter information
Data resolution: 30-second sampling
Trend tables: 1-, 5-, 15-, 30-, or 60-minute display formats
Trend graphs: 1-, 2-, 4-, 8-, 12-, or 24-hour display formats
Electrical Specifications
Power requirements: 100 Vac at 2.5A 240 Vac at 1.3A
Mains frequency: 50/60 HZ
Protection Class: Class 1 per IEC 601-1
Internal battery
Battery type: Lead acid
Battery capacity: 20 minutes
Charging time: 3.5 hours at 25C
Environmental Requirements
Temperature range
Operating: 10C to 45C
Storage: -15C to 50C
Atmospheric pressure
Operating: 525 to 795 mmHg
(70 to 106 kPa)
Storage: 375 to 795 mmHg
(50 to 106 kPa)
TE
Demonstration is a must
AMC / CMC : with spares should be be quoted for five years after expiry of five years warranty
period
Should be FDA or CE certified
The ANAESTHESIA WORK STATION should not remain faulty/inoperational for more than 24 hours i.e.
DOWNTIME 24 HOURS. If it exceeds, the warranty shall correspondingly increase by the same time.
Also an Anesthesia work station of similar quality shall also be made available so that patient care does not
suffer.
Q-1(223)M&E/09
S.NO.
1.
2
3
4.
5
DESCRIPTION
Towel clip
Allis tissue forceps
Needle Holder
Mayo scissor
Pickup forceps
QTY
24
06
04
02
06
6
7
8
9
10
11
Metz scissor
Suction tip
Scalpel Holder short/long
Bab cock
Satin sky type clamp
Aortic cross clamp
04
04
04
04
04
04
12
LA retractor
04
13
Needle Holder
Needle Holder Long
04
04
14
15
16
04
04
03
17
Vascular forceps
04
18.
02
19
20
21
Mosquito forceps
Artery forceps
Kocker forceps
24
24
22
Lung retractor
23
SPECIFICATION
11cm
11cm long 4X5 teeth
(2) 14cm & (2) 16 cm
17cm curved
19.5cm
(3) , 1.5mm tip & (3) mm tip
20cm length, curved blades
(2) 24cm & (2) 30cm yankaocer
12cm & 4(16cm)
10mm tip X 6 length
(2) 25cm & (2) 20cm
(2) 24 cm length, curved &(2) 30cm
length
(2) 26.5cm & (2) 27cm Blade
45X30cm
20 cm
2 rider 18cm<jaw 1.5mm-3 Debaky
jaw 2mm-3 length 19.5-20 cm
24cm, 2mm tip
(2) 20cm & (2) 4cm
15cm long with ratchet with curved
handle Diamond dust straight long
3-19 cm long with ratchet with
curved handle, straight, and
diamond dust.
(2) 15cm 0.4mm tip and (2) 18cm
0.8mm tip diamond dust
18cm long circle 0.5X10 &
1.3X20mm
24-10cm(12 straight & 12 curved)
14cm(12 straight,12 curved)
(12 straight 6-16 cm & 6-18 cm)(12
curved 6-16cm & 6-18cm)
(2)-32cm length 54cm width blade
(2)26cm long & 40 mm width blade
20cm, tip 14mm
24
25
26
Russian forceps
Self retaining mastoid retractor
4
4
27
28.
2
4
29
30
31.
32
33.
34
2
2
2
2
4
2
35.
36.
37
Bone Nibbler
Debakey Angular forceps
Becks vascular clamp
Derra vascular clamp
Debakay multi purpose clamp
Debakay Dissecting & ligation
forceps
Sponge Holder
HLM Tube Holder
Tube milker
2
2
2
10 length
(1) Adult & (1) Pediatric
(1) Teflon roller wheel and (1) steel
roller wheel.
38
Endarterectomy dissector
04
39
40
41
Vascular sling
IMA Needle
Probe coronary
5
10
08
42
43
Spring scissor
44
2
2
2
6
4
45
46
47
48
49
50
51
52
53
2
12
12
10
4
4
54
55
56
57
IMA retractor
Demonstration is a must.
Five-year replacement guarantee and two years warranty.
Q-1(224)M&E/09
SPECIFICATIONS FOR HIGH END LIVE 3D ECHOCARDIOGRAPHY COLOUR DOPPLER SYSTEM WITH TRANSESOPHAGEAL
ECHOCARDIOGRAPHY(TEE)-01 No.
1. System should be a premium end Echocardiography Colour Doppler system with highly
advanced architecture to process multiple data stream simultaneously and in real time for
revolutionary 2D and 3D imaging.
2. System should have 50,000 or more digitally scalable channels for simultaneous formation,
acquisition and processing of multiple ultrasound beams and has a system architecture to
process an entire bandwidth of frequencies from 1 MHz to 17 MHz. System should support
pulse coding and pulse shaping technologies.
3. System should have a dynamic range of minimus 180 dB so that variety of patient sizes can be
handled without compromise.
4. System should have w
5. Extremely high Resolution 2D Imaging, Colour Flow Imaging, M mode, PW Doppler, CW
Doppler, Duplex & Triplex Modes.
6. Should have good Tissue Harmonic Imaging for improved Image quality with quantification.
7. Should offer a frame rate of 500 frames per second or more.
8. Should have the state of the art Transmit Real Time Compound Imaging Technology with
Multiple transmitted lines of sight, for improved visualization and better Image quality in
Vascular Imaging and to virtually clean up the Image of artifacts.
9. Should have advanced Image Processing algorithms to analyse between targets and artifacts
so as to sharpen target anatomy and reduce the speckle and artifacts for improved Image
quality.
10. Should have Extended field of view Imaging of structures, by continuously scanning and
moving the Probe over the area of Interest.
11. Integrated Stress Echo facility to perform Stress Echo Exams
12. System should offer complete on board 2D quantification including TDI of 250 fps. Strain
quantification with capability of drawing 3M-lines at a time and capable of dividing each Mline into 8 sub regions according to user defined sub region sizes
13. Should also have advanced 2D quantification package, IMT quantification, etc.
14. Should have onboard workstation for storage and review of all exams,2D,3D Images, loops
etc.
15. System should be capable of supporting LIVE 3D Matrix Array Transducer. Please mention
3D Data processing speed in technical bid.
16. System should be capable of LIVE 3D with color, enabling users to look at color flow in 3D
with capabilities to crop, rotate, suppress colour, suppress B/W Image, suppress baseline and
change gains. LIVE 3D with colour should be demonstrated with these capablilities at the time
of technical evalution.
-217. System should offer accurate 3D LV volumes and 3D ejection by using all 3D voxel
information, eliminating motion artefacts all geometric assumption. System should offer 3D
synchronicity to measure and compare timing of maximum contraction of regional LV
volumes to determine those patients who will best benefit CRT system. Should display global
LV volume and should provide simultaneous display of 17 regional volume waveform.
18. System should offer Live X-plane imaging with manipulation of orthogonal planelateral,elevation and rotation should be possible. Elevation beam steering should be possible
so that ideal en-face views for measurements can be obtained without moving the transducer.
19. System should offer exclusive human centered design dramatically reducing many of the
known cause of muscle strain and repetitive stress injuries,with ultra bright thickness LCD flat
panel display 20 Monitor with nearly infinite priority adjustment, ability to move the entire
control panel up and down with a single button.
20. Should have DICOM 3.0 for modality, worklist, perform procedure set up, storage commit,
built in the system to be able to connect to Hospital network, Laser Cameras etc.
21. System should have inbuilt Image management facility with facility for direct storage of
Images and loops in the Hard Disk Drive and also thumbnail review to view and edit Images,
loops and also reports.
22. System should have storage facility of images, loops in the hard disk drive of 160 GB or more.
System should be able to transfer Images and clips to CD and DVD media.
23. System should be offered with a workstation for Image and information management that
supports image import, viewing, reporting and storage. Should be able to export images aqs
AVI,BMP,or DICOM in CD/DVD format.
24. Should be offered with the following:
A.
B.
C.
D.
E.
F.
G.
H.
I.
-325. The quoted model should be latest and more recent. Supplier should specifically under
this.
1. Specifications are subject to improvisation prior to finalization.
2. Equipment shall confirm as per latest technology available and
marketed in India during last one year, and as per equipment
supplied at accepted Indian Centres of excellence in Cardiac care.
26. Should have 5 years guarantee + 5 years comprehensive warranty
27. Company should make sure that after getting the complaint that instrument is non
functional/ malfunctional (telephonically or else) instrument must be functional within
24 hours and this period should be deducted from the warranty period or the company
will provide the replacement of same or higher configuration equipment.
28. Demonstration is a must.
Q-1(225)M&E/09
1. Fully automatic single door high pressure steam sterilizer with chamber volume greater
than 70L.
2. Integrated steam generator and two level water ring vacuum pump with water saving
mechanism and silent operation.
3. Sterilization chamber, doors and chamber jacket should be made of high quality AISI 316
Ti steel. Vertical sliding door with safety locks, manual actuation of doors and automatic
door sealing.
4. Should have two microprocessor control system for fully independent checking and control
of the sterilization system. Integrated thermal printer. Should be complete auto diagnostic
system providing error codes on display in case of failure.
5. Absolute pressure sensor for the precise recording and control of vacuum and pressure in
the chamber and additionally in the jacket.
6. Resistance temperature sensors PT100 for the precise control, evaluation and regulation of
the temperature course.
7. Integrated waste water cooling, integrated water saving device, LC display, Chip card
reader and RS 232 interface.
8. Sterilization to be achieved at 134 degrees. The sterilizer should have at least 4 preloaded
programs for standard sterilization, pre-heating, containers and rubbers. It should also have
preloaded test programs for Bowie-Dick test and Vacuum test. Should have the option to
load customer specific programs in the sterilizer using chip card.
9. The sterilizer should come with standard accessories like sterilization baskets, basic insert,
guiding rail for rack, grid tray, start up kit, etc.
10. Should be ISO, CE, TUV certified and should comply with EN 285 and EN 554 standards.
11. Should have 5 years guarantee + 5 years comprehensive warranty.
12. Company should make sure that after getting the complaint that instrument is non
functional/ malfunctional (telephonically or else) instrument must be functional within 24
hours or the company will provide the replacement of same or higher configuration
equipment.
13. Demonstration is a must.
Q-1(226)M&E/09
WASHER DISINFECTOR
The automatic washer disinfector with efficient cleaning & disinfecting system before
sterilization process for reusable large & small instruments , trays, glassware, shoes, Anaesthesia /
respiratory goods, bedpans and urinals etc. with double sliding doors. Also suitable for
disinfecting rigid MIS instruments accessories.
Automatically controlled, double walled made of St. Steel, Washer / Disinfector with rotary
spray assemblies and two automatic vertical sliding doors having tinted tempered glassone
door for loading racks with soiled items and second door on clean side for taking out washed
and cleaned racks
Chamber Load capacity approx. 230 to 250 Liters
The sliding doors should be configurable for automatic or manual operation and should be
interlocked to prevent cross-contamination.
Should be having low consumption of water with maximum 40-45mins. Cycle timing with
dispenser system for one enzyme; three detergent and one lubricant pumps and having heaters
to heat water
Should have HEPA Filtered Drying arrangement through compressed air and should have
electrical heating coil for drying cycle.
Q-1(227)M&E/09
Automatically controlled St. Steel cabinet type ULTRASONIC cleaner with four lockable
castors.
Having automatic opening lids and safe instrument loading trays in the dual tanks of not less
than 40 Liter capacity
Should be able to hold min. 10kg weight of the instruments
To achieve high degree of fast and efficient cleaning, the ultrasonic waves generators in the
wash tank should provide min. 750 Watts of sonic power and transducers should not be
operating at less than 100kHz
Should also be possible to flush ultrasonically atleast five Rigid Lumens of surgical scopes.
Should have facility to inject instrument lubrication spray automatically during rinse.
Should have inlet provision for Hot & Cold water and compressed air (to aid drying).
Automatic cycling and indicating completion visually and audibly along with automatic lid
opening at the end of timed cycle.
Lid should be electrically operatable with foot actuated switch.
Cycle to stop on accidental lifting of the lid
Provide four trays with tray hooks to hold instruments and two port flushing kit for rigid
lumens with each cabinet
Provide six months supply of suitable Instrument Lubricant (4packs) and Enzyme based
chemical cleaner (8 packs) with each supply.
Electrical Service 220 VAC,50 Hz
Standard: Should meet applicable UL / CSA /CE standards
The manufacturing firm should have own trained service engineers based in Delhi NCR .
Q-1(228)M&E/09
Specification for Electrical Steam Generator to meet the requirement of steam for Sterilizers
Salient Features
a. Vessel type boiler fitted with pressure Stat, Steam Trap, Safety Valves,
Pressure Gauges, Low level Water sensor.
'
b. Fully insulated with glass wool covered with metallic covering to meet the
requirement of steam for the sterilizers both in Gynae O.T.& M.T.P. O.T .
Q-1(229)M&E/09
For over 300 bedded Hospital with min. 5 to max. 15 OTs and approx. 50 to 70 ICU beds and
having capacity for high processing of loads (approx. 32 to 35cu.ft /900-1000 Litres)
Microprocessor controlled steam under pressure , free standing sterilizer
The Sterilizer having adjustable each cycle time should not be more than 60 minutes
Having single nickel clad o.63mm thick hot-rolled carbon steel manual door with st. steel
hinges and warranted long life , non-lubricated steam activated door seal(gasket) . (Optionally
also offer double door unit)
Autoclave should also be able to perform Bowie & Dick test and vacuum leak test.
Automatic cycling & drying and indicating completion both, visually and audibly.
Equipped with pre-vacuum; gravity & also Liquid cycles.
Having electronic water saving control condensing the exhaust chamber steam with excellent
drain system preventing pollutants to enter water supply.
Having touch sensitive screen with LED/LCD controls with battery back-up and digital
thermal printer as standard for records keeping.
Having inbuilt Vacuum pump and electro solenoids valve controls .
No extra air compressor should be part for operations , all controls should be through electrical
solenoid valves as part of autoclave.
Having pre-programmed operational parameters which can be adjusted for specific
applications by the user and emergency manual exhaust valve.
For steam sterilisation - to be adjustable from 250o F (121 o C) to 270o F(134 o C)
Chamber Type: DOUBLE JACKETED , either Cylindrical or Rectangular St Steel chamber ,
approx. 26 X37x 60 (Capacity- 900 to 1000 litres)
The panel should include various pressure & temperature display gauges for depiction of actual
pressure/ temperature in chamber, jacket and on gasket.
Water consumption not more than 15 lpm with electronic water saving controls
Standard: Conforming to FDA and ASME Pressure Vessel and others e.g.
UL /CE/ CSA
Electrical Service 240 VAC,50 Hz
Accessories to include: -Loading Cart & Carriages etc.
Sterility assurance and protective barrier products and compatible validation process should
also be provided with supplies for 300 cycles.
Provide electric steam generator providing quality steam i.e. condensate free , 97 to 100%
saturated vapour complete with piping ; valves and pressure relief etc. delivery at 50 to 80 psig
pressure.
The steam generator pressure vessel should be ASME Grade Carbon Steel rated for
100 psig (690 kPa) with Water-level Control ,iIn addition, power to shut off to two
heating elements of 32.5KW each if water in the heating section should fall below a
preset level. System supply valve should be rated to withstand hydrostatic test of 300
psig
The steam generator to have a water level sight glass with upper and lower handvalve shutoffs.
The manufacturing firm should have spares availability in India and must have own trained
service engineers based in Delhi NCR .
Water softner plant to be provided along with sterilizer/main equipment.
To be supplied with compact steam sterilizer, specification attached in annexure c
ANNEXER C
Autoclave should be suitable for the use in Room adjacent to OTs/ICU for flash sterilization of wrapped
instruments, unwrapped instruments etc. with temp. control 100 to 137C
Autoclave should also be able to perform Bowie & Dick test and vacuum leak test.
The autoclave should be completely microprocessor controlled with real time printing device to record events
during the propagation of cycle.
Autoclave should have prevacuum, gravity and flash cycles and having internal battery facility in case the
microprocessor control fails as backup up for all cycle memory so that proper cycle completion occurs on power
restoration.
The double jacket chamber and door should be made of heavy duty stainless steel type 316 L . Fully automatic
horizontal Sliding door ,made of 316L steel.
The Pipes and the fittings should be made of stainless steel and brass.
The panel should include various pressure & temperature display gauges for depiction of actual pressure/
temperature in chamber, jacket and on gasket.
Trolley made of stainless steel should be included to transfer carriage from autoclave.
At least four line LCD/LED display with numeric and touch screen command keys to be the part of autoclave.
All interrupts and failures must be indicated through audio visual alarms and recording.
The autoclave should include all safety features like solenoid safety valves, current overload relay, contactors
etc.
Air to be drawn from chamber through vacuum pump and relived to atmosphere through bacteria retentive filters
.
Inbuilt Steam Generator of adequate capacity should be included to feed steam to Autoclave.
The autoclave adjustable each cycle time should not be more than 45 minutes if the flash cycle if autoclave
operates at the working temperature (inner chamber) of 134C at a pressure of 15 pounds per square inch (psi) .
Adequate service back up is required during the warranty and the period of after warranty is over.
Autoclave should meet international standards such as ASME, EMC directive, CSA and UL and should be as per
CE machine directives. The quality system should also be certified in compliance with ISO 9001:2000.
Q-1(230)M&E/09
Control system to monitor and controls all sterilizer operations and functions with
cycle time of less than 1 hour.
Control system to be factory programmed with standard sterilizing cycles with
Touch screen controls for Cycle sterilize time and aeration time can be user
adjusted
Having Ink on Paper impact Printer with Ethernet port for remote monitoring
Safety Features-Visual and Audible Alarms for abnormal deviations and end of
Cycle .
The sterilant H2O2 cartridge should be for minimum 15 cycles and 45 cartridges
with the shelf life of more than 09months should be supplied with the unit.
Sterility assurance and protective barrier products and compatible validation
process should also be provided
Electrically operateable on 440V, 3 phase 50 Hz supply.
The manufacturing firm should have own trained service engineers based in Delhi
NCR .
Q-1(231)M&E/09
Endovision single chip camera with IPM (Integrated image processing module).Focal length
should be 25mm-50mm.It should have high horizontal image resolution more than 250 lines and
also should integrate parfocal zoom lens.It should have 2 programmable function key in the
camera head for control of camera function,video printer/recorder function. It should have
automatic white balance with memory function. It should have alternatively manual or automatic
digital exposure control,weight of control unit 2.95 kg(approx) ,power supply 100-240 VAC,50/60
Hz.It should be supplied with following accessories:BNC connecting cables, S-VHS connecting cable, RGB sync connecting cable, set and keyboard
for character generator and control of camera functions or any upgraded recording system.
Specifications:
Image sensor: CCD chip
Min. sensitivity : 3 lux
Q-1(233)M&E/09
Disposable Neonatal Cuffs - 2.5 cm, 3 cm, 4 cm & 5cm, 1 no. each
Q-1(234)M&E/09
Q-1(235)M&E/09
Q-1(237)M&E/09
Technical Specifications
Size:
- Over all
- Chamber
Electrical :
- Supply
- Loading
Construction
Instrumentation
Safety
Sterilizing
- Sterilizing time
- Typical overall time
- Drying time
Operating Pressure
Q-1(238)M&E/09
Q-1(239)M&E/09
14. Alarms should be audio-visual and should have automatic and manual alarm setting for all
parameters.
15. Should display alphanumeric alarm messages and should have alarm lamp at top for clear
visibility from distance.
16. Should have Inbuilt rechargeable battery (2 hars. Operation), with on screen battery status
indicator.
17. Should have inbuilt thermal printer with selectable printing speed 50, 25, 12.5, 6.25mm
/sec.
18. Should have a card slot for storage of arrhythmia data & maintenance purposes.
19. All Cable connections should be at side of the monitor for easy connections &
disconnections of the probes.
20. Should be compatible with central monitor station through Wireless Telemetry.
21. Should meet international quality directives such as CE, ISO, 9001 & ISO 14001.
22. Supplied complete with
* Cuff for Adult : 12cm & Child : 9 Cm, 1 no. each
* Disposable Neonatal Cuffs 2.5 cm, 3 cm, 4 cm, & 5cm, 1 no.each
* Cuff Hose for reusable & disposal cuffs, 1 no.each
* Temperature Probe (Rectal), 1 no.
* ECG Lead Wires (5 lead) with cable, 1 no.
* SpO2 Sensor (finger) with extension cable, 1 no.
Q-1(241)M&E/09
ECG Monitor with Defribrillator with Oxygen saturation & NIBP Monitoring
1.Defibrillator Monitor Recorder should be lightweight.
2.Biphasic, Latest model, with auto and manual mode. Manual selection upto 360 J.
3.Should be mains and battery operated, with charging indicator.
4.Should be able to deliver 30 shocks with fully charged battery.
5.Should have true 1-2-3 Color-coded operations.
6.Should have inbuilt Internal Thermal Recorder.
7.Pulse oximetry and NIBP as Integral part of the unit.
8.Should have Automatic lead switching to see patient ECG through paddles or leads. Should
measure chest impedance and should be able to compensate.
9.Should have Defibrillator testing facility.
10. Should be provided with Adult and Pediatric external paddles.
11. Should have both Synchronous and Asynchronous mode.
12. The charging time to highest every level should be less than 3 seconds.
13. Disposable defibrillator pads 10 nos with each machine
14. Complete set of ECG leads-2nos
15. NIBP cuffs with each machine
a. Adult 2 cuffs
b. Child 2 cuffs
c. Infant 2 cuffs
16. Pulse oximeter Probes with each machine
a. Finger probes Adult 2 in no.
b. Ear probe 2 in no.
17. Compliance Report to be submitted in a tabulated and point wise manner clearly
mentioning the page/para number of original catalogue/datasheet
18. Should have local service facility.
19. Demonstration is must.
20. Guarantee for two years
21. AMC for 5 years after guarantee.
Q-1(242)M&E/09
Q-1(243)M&E/09
Q-1(244)M&E/09
Q-1(245)M&E/09
Q-1(246)M&E/09
TECHNICAL SPECIFICATIONS FOR CELL WASHING
SHOULD HAVE
OPERATION.
FOUR
SPEED
BRUSHLESS
INDUCTIONS
MOTOR
FOR
QUIET
Suitable UPS.
Working manual.
Equipment should be complete in all aspects to start working from day one.
Q-1(247)M&E/09
Two
5000 approximate
Max. ref. Gm
5000 approximate
Head
Tube capacity
Main unit
:
Cabinet made of sheet steel corrosion
resistant Cover made of acrylic see through
with interlook.
Control Panel
:
Start, stop switches stepless speed regulat
zero Start switch continuous ready digital
tachometer. Automatic timer & cut off.
Digital speed meter ommeter, unbalance
switch and Dynamic brake switch.
Should include all accessories required to centrifugation of 28x 15 ml glass tube or more tubes.
Guarantee
Two years.
Q-1(248)M&E/09
SHOULD BE STURDY ONE PIECE DRAWERS WITH HOLES FOR COMPELETE AIR CIRCULATION
ACROSS BOTH SURFACES OF PALATELET BAGS
SHOULD HAVE DELRIN ROLLERS AND GLIDES FOR THE DRAWER STORAGE PLATFORM TO
AGITATE SMOOTHLY.
Suitable UPS.
Working manual.
Equipment should be complete in all aspects to start working from day one.
Q-1(249)M&E/09
Q-1(250)M&E/09
.3 kg.
Dimensions should be 7.5 in. (20cmLx (11cm) W x 1.75 in (5cm) H.
5 years comprehensive warranty.
Free installation at user site.
Standard accessories as per catalogues
Suitable UPS.
FDA and CE Certification
Working manual.
Should have authorized service centre in New Delhi/Delhi.
Equipment should be complete in all aspects to start working from day one.
Q-1(251)M&E/09
Q-1(252)M&E/09
PLATELET INCUBATOR SHOULD HAVE THE PROVISION TO STORE THE AGITATOR FOR 48
PLATELET BAGS AGITATOR.
SHOULD HAVE CLEAR VIEW SINGLE PANE TEMPERED GLASS ROLL OUT DOOR WHICH
SHOULD ROLL INSIDE THE CHAMBER FOR OPENING OF THE INCUBATOR .
SHOULD HAVE PROVISION FOR 47DAY INKLESS CHART RECORDER WITH BATTERY
BACKUP FOR CONTINEOUS OPERATION DURING POWER FAILURE.
Suitable UPS.
Working manual.
Equipment should be complete in all aspects to start working from day one.
Q-1(253)M&E/09
TECHNICAL SPECIFICATION OF PLASMA THAWING SYSTEM
Q-1(254)M&E/09
Q-1(255)M&E/09
Q-1(256)M&E/09
3.
1.
Fully automatic, open system with capacity to perform four micro plate
simultaneously.
2.
Should have the capacity to load up to 90 samples with option of adding an
additional rack up to 150 samples.
3.
Should be able to perform dilution procedure of test samples.
4.
Should have an option of serial or parallel modes.
5.
Should have 8 or 12 way pipetting direction.
6.
Should have 8 way washing by strip or plate mode.
7.
Should have sampling capability both by disposable tips and Teflon coated metal needle.
8.
Disposable tips capacity should be minimum 115 tips with the option of adding
additional tip rack.
9.
Built in liquid level detector for samples/reagents and buffers.
10.
Should have micro strip and dispense check.
11.
Dead volume reagent and sample should be more than 200 microlitres.
12.
Should have two pipetting arms.
13.
Should have two incubators with a variable temperature from room temperature to
45o C + 1o C.
14.
Incubator should have sandwich dry incubation to avoid evaporation.
15.
Should not require plate sealers.
16.
System should dispense back the balance reagents in the reagents vial after
pipetting
to avoid all wastage.
17.
Should have two built in reader with halogen lamp.
18.
Expandable work load from two micro plate to eight by connecting four additional
modules.
19.
System should have five filters, ranging from 400mm to 700mm with the option of
adding additional modules.
20.
Should able to read all types of micro plate (U,V or flat)
21.
Plate shaking option before reading and during incubation.
22.
Should have a waste disposable system with the waste tank capacity of 3 liters.
23.
Should have built in diagnostic at start up.
24.
Should have a memory capacity for 500 protocols and 500 profile.
25.
Should be able to perform 6 assays per system per run.
26.
Software should be capable to operate under windows atmosphere.
27.
Should have the facility for LID, MIMS interfacing.
28.
Should have the facility to read qualitative and quantitative assays.
29.
Service software should be built in.
30.
Should have GPL features built in:All actions and problems automatically logged on.
QC and test validation.
Daily, weekly and monthly maintenance.
31.
32.
33.
34.
35.
Q-1(257)M&E/09
Q-1(258)M&E/09
Q-1(259)M&E/09
Visibility
Washing system
7.
Shaking
8.
9.
Liquid sensors
10.
11.
12.
Up-gradability
13.
Compliance
14.
15.
16.
17.
18.
19.
20.
Q-1(260)M&E/09
Extraction forceps
1. No.17, serrated English pattern right upper molar, made of stainless steel
- 15
2. No.18, serrated English pattern left upper molar, made of stainless steel
- 15
3. No.67, Serrated English pattern upper third molar, made of stainless steel
- 10
- 10
- 5
- 10
- 10
- 25
- 25
10. No. 79, Serrated English pattern lower third molar, made of stainless steel
- 5
11. No.13, Serrated English pattern lower anterior, made of stainless steel
- 10
12. No.74, Serrated English pattern lower root, made of stainless steel
- 15
13. No.75, Serrated English pattern lower bicuspid, made of stainless steel
- 10
14. No.74XN, Serrated English pattern lower root (narrow beak), made of
stainless steel
- 10
15. No.kI-1, Serrated English pattern lower incisor anterior, made of stainless steel
- 10
16. No.kI-2, Serrated English pattern lower molar, made of stainless steel
- 10
17. No.kI-4, Serrated English pattern upper molar, made of stainless steel
- 10
18. No.kI-5, Serrated English pattern upper anterior, made of stainless steel
- 10
7. No.3 Goldfogel composite contouring instrument with aluminium titanium nitride coating
5
B. Tissue pliers
1. Adson plain tissue plier of Perma sharp variety with tungsten carbide inserts (12cms)
2
2. Adson 1X2 straight jawed tissue pliers of Perma sharp variety
with tungsten carbide inserts 12cms
2
3. Angled Cushing tissue plier of Perma sharp variety (18cms)
10
4. Goldman Fox straight 13 cms with tungsten carbide tips
15
C. Calipers
1. Weiss modified castroviejo calipers, 0-40mm (17cms)
1
D. Cheek retractor
1. Orringer cheek retractor, medium, made of immunity steel(corrosion resistant)/equivalent
5
2. Weider cheek and tongue retractor (small),
made of immunity steel(corrosion resistant)/equivalent
3
3. Weider cheek and tongue retractor (large),
made of immunity steel(corrosion resistant)/equivalent
3
4. Posterior Arens tissue retractor (serrated)
2
E. Mouth Prop
1. Markel small child latex free mouth prop
2
F. Mixing cup
1. Modified pumice cup, made of immunity steel/equivalent
2
G. Probes
1.
H. Filling instruments
1. No. 18 Ball burnisher with immunity steel (corrosion resistant)handle/equivalent
20
2. Cement spatula
10
3. Amalgam condenser
25
4. Amalgam carrier
15
5. Plastic filling instruments
30
I. Other Instruments
1. Mouth gag with adult size ratchet design
5
2. No. CSI-1 Non serrated cord packer
2
3. Implant Retractor
2
All bidders should supply original catalogue of quoted instruments along with
the necessary documents
Q-1(262)M&E/09
Q-1(263)M&E/09
The autoclave should provide sterilization at 121o C and 134o C for both wrapped and
unwrapped tools and also a flash cycle for rapid sterilization.
The autoclave should be equipped with a powerful vacuum pump to eject air pockets from
the chamber at the beginning and at the end of cycle (Pre-vacuum and Post vacuum)
Water purification unit (based on reverse osmosis principle) should be supplied along with the
autoclave, and it should be possible to connect the water purification unit directly to autoclave for
supply of high quality demineralized water.
It should have minimum four sterilization programs and two test program. Programs should be
monitored by microprocessor.
It should be class B autoclave so that hollow bodied instruments, handpieces, and turbines can
be fully autoclaved.
The system should comply with International Standards for sterilization , should be CE marked
and manufactured by ISO certified company.
Q-1(264)M&E/09
Q-1(265)M&E/09
Dental Chair
Dental Unit
Operating light
It should have latest foot operated LED/halogen Light (min 35,000 LUX)
Spittoon/Water unit
Programmes
Dental Stool
Two No.s
It should be provided with one doctors stool and one assistants stool with adjustable backrest
tilt including an adjustable ring for foot rest.
Compressor
Oil free medical grade compressor of 1.0 HP (fully imported)
The company manufacturing these chairs should be an ISO certified and products should
be C.E marked
All the accessories supplied should be of same manufacturer
Price should be inclusive of 5 years AMC after warranty period
Q-1(266)M&E/09
Dental Elevators
1. Warwick James straight elevator with Non slip grip handle,
made of stainless immunity steel/ equivalent
10
10
10
10
15
15
20
20
9. 12 LX cryer Elevator with cross bar handle with Non slip grip handle,
made of stainless immunity steel/ equivalent
15
10. 12 RX cryer Elevator with cross bar handle with Non slip grip handle,
made of stainless immunity steel/ equivalent
15
11. No.1L Seldin cryer elevator with Non slip grip handle,
made of stainless immunity steel/ equivalent
10
12. No.1R Seldin cryer elevator with Non slip grip handle,
made of stainless immunity steel/ equivalent
10
14. No. 1 Howard Root tip picker with Non slip grip handle,
made of stainless immunity steel/ equivalent
10
10
10
17. No.1 Heidbrink root tip picker with Non slip grip handle,
made of stainless immunity steel/ equivalent
10
19. No. 44C Bradley elevator with Non slip grip handle,
made of stainless immunity steel/ equivalent
Q-1(267)M&E/09
Q-1(268)M&E/09
Q-1(269)M&E/09
The feedwater should be tested by the company/firm and if needed a pre-filtration system
should also be installed to improve the feed water so that the durability of the
cartridge
is
increased.
ANALYT1CAL GRADE WATER SYSTEM:
The final purification step should involve a self regenerating Electro deionization module
for chemical ion exchange regeneration.
3.
Conductivity meter should be present before and after the RO cartridge to monitor RO
cartridge efficiency.
4.
Product water quality- Resistivity typically up to l0-l5Megohmcm,TOC:<30ppb,Flow
rate 3L/hr, CONDUCTIVITY <0.2uS/cm, Silicate Removal
> 99,9%.
ULTRAPURE WATER SYSTEM
1.
2.
3.
4.
Three stage purification process with initial purification packs tailored for specific
feed water, an application specific ultrapure cartridge and an absolute 0.22 micron
PVDF membrane final filter in stacked configuration.
The system should be capable of removing both inorganics and organics and ideal
for molecular biology including PCR, electrophoresis and cell tissue culture.
The resistively cell should be coaxial with a cell constant of minimum 0.0lcm
The system should have a built-in RS232 port,a low voltage DC pump, automatic
recirculation, an alphanumeric backlit LCD display with autodiagnostic features and
alarms.
5.
The ultrafilter membrane of the system should have at least 5000 dalton
weight.
6.
The system should have a flexible rocker arm for dispensing water, to make it
friendly.
7.
The system should have a facility for volumetric dispensing as an option, with
upto I litres/ mm.
8.
Product water quality- Resistivity- 18.2 Meg-ohm, bacteria < lcfu/ml, TOC 5-10
Particulates <1/mI, Pyrogen levels <0.001 EU/rn!, Flow rate approx 1.0
I/mm.
9.
It should be from a licensed company and should be ISO /ISI or equivalent
10.
All consumables (including the cartridge) should be provided for a period of two
molecular
user
low rate
ppb,
certified.
years.
11.
12.
13.
14.
Q-1(270)M&E/09
Maximum RCF: at least 4,500xg Swing out at least 21,000xg Angle Head
Centrifuge must be capable to spin minimum 16 standard micro plates with max RCF of 3,700xg or
more in one run
Centrifuge must be capable to spin 2 DNA/RNA Filter plates upto 85 mm with max RCF of
5,800xg or more in one run
Q-1(271)M&E/09
Q-1(272)M&E/09
Q-1(273)M&E/09
2. MICROSCOPE
3. CONDENSER
W.D. 72mm)
contrastring slits included
4. IIIUMINATION
5. STAGE
6. OBJECTIVES
approximately 18.5)
10X/0.25, W.D. approxima
7. FILTERS
8. OBSERVATION TUBE
9. EYEPIECE
Q-1(275)M&E/09
Q-1(276)M&E/09
Q-1(277)M&E/09
Q-1(278)M&E/09
36. There should be glass thermometer fitted for observing the temperature.
37. Air ventilator ports should be provided .
38. There should be air circulation fan .
39. Control Panel- equipment should be provided with a panel having a thermostat control
knob. ON/OFF switch , pilot indication light and provision for fixing the Timer .
40. Inbuilt User settable Audio / Visual Alarm in case of temperature over shoot .
41. Power requirement - should be supplied with a cord and plug . Suitable to operate on 220
V single phase ,50 Hz , AC Supply .
42. 2 years warranty followed by three year CMC
43. . ISI or equivalent certification
Q-1(279)M&E/09
Electronic Balance
Technical Specifications:
1. Microprocessor based single pan top loading Analytical Balance
2. High accuracy & precision
3. Weigh accurately up to 3rd decimal place
4. Auto self-calibration facility
5. Auto zero Setting
6. One touch calibration
7. Weighing capacity up to 120g
8. Readability and repeatability 0.001g
9. Stabilization time < 5 second
10. Liquid Crystal Display (LCD) for display
11. Power 220-240 V; 50/60 Hz
12. 2year warranty followed by three year CMC
Q-1(281)M&E/09
Micro centrifuge
Technical Specification:
1. Light in weight and compact in size Approx. 15x25x20 cm (6x10x8) inches .
2. Should be suitable for PCR work,
3. RPM 5,000-14,000 with increment of 100 RPM
4. RCF 1700-14,500xg with increment of 100xg
5. LED Display for time, RPM & RCF
6. Noise Level < 56db
7. Hold at least 12 tube of 0.2/0.5/2ml
8. Quick Spin mode and one knob adjustment to change parameter
9. Power 220-240 V; 50/60 Hz
10. Safety Features: Imbalance Detection, lid interlock, over speed etc.
11. Power Supply 220-240V;50/60 Hz
12. ISI/ISO or equivalent Certified,
13. Warranty Period of 2 Years, subsequent 5 years comprehensive AMC
14. The instrument should be functional from the day one
Q-1(282)M&E/09
Q-1(283)M&E/09
Q-1(284)M&E/09
Q-1(285)M&E/09
Q-1(286)M&E/09
Q-1(287)M&E/09
48. The gap between the two walls should be filled with special grade glass wool for proper
insulation and to avoid heat losses.
49. Inner chamber to be fabricated with ribs to adjust shelves to any convenient height .
50. Polished SS sheet removable shelves minimum three.
51. Insulated door fitted with heavy hinges with a ball catcher spring-loaded door closing
device.
52. Door gasket made of synthetic rubber .
53. Heating element should be of high grade imported nichrome wire which are insulated and
should give uniform temperature all over the space .
54. Temperature control by an electronic digital temperature controller cum indicator
55. Temperature range 40 to 250 degree C + 5 degree C
56. Temperature accuracy of 0.1 Degree C @ 25 degree C.
57. There should be glass thermometer fitted for observing the temperature.
58. Air ventilator ports should be provided .
59. There should be air circulation fan .
60. Control Panel- equipment should be provided with a panel having a thermostat control
knob. ON/OFF switch , pilot indication light and provision for fixing the Timer .
61. Inbuilt User settable Audio / Visual Alarm in case of temperature over shoot .
62. Power requirement - should be supplied with a cord and plug . Suitable to operate on 220
V single phase ,50 Hz , AC Supply .
63. 2 years warranty followed by three year CMC .
64. ISI or equivalent marking .
Q-1(288)M&E/09
Q-1(289)M&E/09
Q-1(291)M&E/09
Q-1(292)M&E/09
Electronic Pipette.
Printer Interface with facility of print out of reports on
Pathology forms.
The analyzer should have a built in display and a built in graphic printer.
Computer connection: R 232.
Automatically calculates results related to the stored calibration curves with the
corresponding units, activity and international normalized ratio. (INR).
Installation and demonstration at place of working.
Working manual
5 yrs warranty
Start up reagents for 1000 tests.
Standard accessories, spares as per catalogues.
Should have authorized dealer /service centre in Delhi.
Equipments should be complete in all aspect to start working from day one including
printing of results.
Quotation for all consumables.
Q-1(294)M&E/09
Q-1(295)M&E/09
storage for 5000 patients information storage and files each with 300 points for QC and
1000 test order information in memory.
Should use Solid Semiconductor laser or lower power consumption, higher stability, and
longer life thereby cutting down on maintenance cost.
Should have an AUTO SAMPLER with cap pierce making it a totally walkway system,
decreasing the manual intervention.
Should have Extensive QC feature, like files for X bar on LJ plot available, One file for X
bar M, provide Delta checks available for cumulative review and an option for online QC.
Firm must have its own Calibrators, Controls and reagents for the Analyser. They should
also provide calibration certificate.
The analyzer should have five years warranty, Reasonable price of AMC to be given after
warranty period.
Should have good installation base in Govt. Hospitals in Delhi and be backed by high
quality support at reasonable cost and unmatched network of well-trained service and
application support staff within NCT of Delhi.
The Analyser should be supplied with UPS of 30 minutes back up.
Should supply standard Blood Mixer along with Analyser.
The system should be supplied with free reagents of 1000 samples including reticulocyte
count and one complete set of calibrators.
5 years comprehensive warranty.
Free installation at user site.
Standard accessories as per catalogue
Suitable UPS.
FDA and CE Certification
Working manual.
Should have authorized service centre in New Delhi/Delhi.
Equipment should be complete in all aspects to start working from day one.
Q-1(296)M&E/09
Q-1(297)M&E/09
Q-1(298)M&E/09
7. Minimum three reagent positions of which minimum two should be refrigerated with
constant stirring.
8. Facility for pre heater.
9. Should accept primary sample tubes. On board bar code reader.
10. Alphanumeric key board.
11. Onboard autodilution.
12. Inbuilt printer.
13. Having liquid level sensor.
14. Capacity to have on board patient data for more than 300 samples also capacity to store
more than 20 QC data files with external printer.
15. Preference to facility of single report printing on
hospital laboratory form.
16. Open system
17. 210-240 V.
18. CE/FDA approved.
19. Installation and demonstration at place of working.
20. Working manual
21. 5 yrs comprehensive warranty
22. Start up reagents for 1000 tests.
23. Standard accessories, spares as per catalogues.
24. Should have authorized dealer /service centre in Delhi.
25. Equipments should be complete in all aspect to start working day one including back up
power pack compatible on line UPS.
26. Quotation for all consumables for next five years.
Q-1(299)M&E/09
Should be fully automated haematology analyzer providing 18 parameters including a 3part differential, with user definable settings for RDW-CV and RDW-SD.
The system should give the Differential count as Lymphocytes, mixed population and
neutrophils while mixed population should include Eosinophils, Basophils and Monicytes.
The system should be capable of processing samples at a speed of 60 samples/hour.
The system should be Sample Rotary Valve(SRV) based for the precise sample alloquoting
for dilutions.
The system should have auto probe wiper to clean the sample probe automatically after
sample aspiration.
The system should use non cyanide based reagent for Hb estimation.
System for the reliability of the results, should have Electrical Impedence method of cell
counting with an integrated temperature sensor for monitoring and compensating for shifts
in room temperature.
The system should use to proven and approved Volumetric Metering system of cell
counting, for WBCs, RBCs AND PLTs for high precision of the results and stability of
the calibration.
The system should have a system of count and aperture monitoring every 0.5 secs for
precision and reliability of the counts.
The system should have automatic floating thresholds for the correct separation of RBCs
and PLTs during overlap in cases of Microcytes/large platelet.
System should not require any daily maintenance except daily shutdown.
The system should automatically give an alarm to the operator for doing the maintenance.
The system should use of reagents only high intensity LED for Hb estimation.
All reagents required should be available locally from the company or its authorized
distributor.
5 years comprehensive warranty.
Free installation at user site.
Standard accessories as per catalogue
Suitable UPS.
FDA and CE Certification
Working manual.
Should have authorized service centre in New Delhi/Delhi.
Equipment should be complete in all aspects to start working from day one.
Q-1(300)M&E/09
H) The jacket would be insulated with glasswool and covered with stainless steel cover.
I) Tray and basket for pre and post sterilization.
The unit would be provided with High Pressure Feed Water Pump for filling of water into the
steam generator when under pressure with interconnecting piping etc.
The unit would be manufactured as per ISI specifications and also would bear ISI certification
Mark IS: 3829(Part- I &II).
OT light should tested for international standard for safety & quality such asIEC 60601-1
IEC60601-2-4
CE marked
Manufacturer should be ISO9001:2000/ISO13485:2003 certified.
Physical demonstration should be made available
Q-1(302)M&E/09
Q-1(303)M&E/09
TECHNICAL SPECIFICATION
ACTIVE/PASSIVE TRAINER FOR UPPER & LOWER LIMBS
Active/ Passive Movement Therapy System for lower limbs and upper limbs.
Should have safety foot shells for feet and leg guides with calf shells to secure support for the
legs.
Q-1(304)M&E/09
Stroke: 2.5 mm
For reciprocating saw blades and rasps
Saw Blade, Usable Length 7.0 mm to 34.5 mm, Blade width 2.9 mm to 6.4 mm, Cutting Thickness
0.60 mm
One Pair Spare Saw Blade of each size
Burr Attachment Straight/Angled
Gear ratio 1:1
Craniotome Attachment and Dura Guards for Neurosurgery
Gear ratio 1:1
Good turning capabilities
3 sizes of dura Guards and corresponding Cranial Burrs
Perforator, Protection Sleeves and Trepan Burrs
Gear reduction 64:1
For safe opening of cranial vault
Irrigation Nozzle for Attachments
For Cooling
Burrs
Burrs, Round, dia 1.0 mm to 8.0 mm
Burrs, Round, Diamond coated, dia 1.0 mm to 6.0 mm
Acorn Burr dia 5.0 mm to 9.0 mm, Head Length 6.7 mm to 10.0 mm
Burr, Egg-shaped, dia 4.0 mm to 5.5 mm, Head Length 8.0 mm to 10.0 mm
Burr, Pear-shaped, dia 4.0 mm to 6.0 mm, Head Length 6.9 mm to 9.7 mm
Burr, Barrel-shaped, dia 4.0 to 6.0 mm, Head Length 90. mm to 11.0 mm
Burr, Tapered fissure, Carbide, dia 1.0 1.6 mm to 2.1 -2.6 mm, Head Length 4.3 mm to 16.0 mm
Burr, Inverted Cone, dia 6.5 mm, Head Length 6.1 mm
Drum Burr, dia 4.7 mm to 9.1 mm, Head Length 7.9 mm
Burr, Circular, Diamond Coated, dia 25.0 mm, Head Length 0.7 mm
Lindemann Reamer, dia 1.8 -2.3 mm, Head Length 20.2 mm
Swanson Burr, dia 2.0 mm to 5.0 mm, Head Length 6.3 mm to 15.8 mm
Burr, Pin-shaped, dia 1.1 1.4 to 3.0 mm, Head Length 6.0 mm to 34.9 mm
Neuro Burr, dia 1.7 mm to 2.9 mm, Head Length 2.3 mm to 3.8 mm
Drill Bit, dia 1.0 mm to 2.5 mm, Head Length 12.0 mm
Wire Pass Drill, dia 1.1 mm to 2.0 mm, Head Length 5.0 mm to 7.0 mm
Cranial Burrs, dia 1.2 1.8 mm to 1.7 -3.0 mm, Usable Length 11.0 to 25.0 mm
Dental Burrs 2.35 mm, Burr Round with Mini Quick Coupling, dia 3.0 mm to 5.0 mm, Total
Length 28.0 mm to 45.0 mm
Burr, Egg-shaped with Mini Quick Coupling, dia 7.0 mm to 8.0 mm, Head Length 4.8 mm to 11.0
mm, Total Length 28.0 mm to 45.0 mm
Burr,Conical with Mini Quick Coupling, dia 5.0 mm to 6.0 mm, Head Length 8.3 mm to 9.7 mm,
Total Length 23.0 mm to 45.0
Burr, Pear-shaped with Mini Quick Coupling, dia 5.0 mm to 6.0 mm, Head Length 8.3 mm to 9.7
mm, Total Length 23.0 mm to 45.0 mm
Burr, Tapered fissure with Mini Quick Coupling, dia 1.0 -2.1 mm to 1.6 3.2 mm, Head Length
11.3 mm to 12.0 mm, Total Length 31.0 mm to 45.0 mm
Burr, Circular with Mini Quick Coupling, dia 8.0 mm to 15.0 mm, Head Length 0.8 mm to 1.0
mm, Total Length 28.0 mm
Lindemann Reamer with Mini Quick Coupling, dia 2.0 2.3 mm, Head Length 35.0 mm, Total
Length 53.0 mm
Burr, Round with J-Latch Coupling, dia 3.0 mm to 5.0 mm, Total Length 28.0 mm to 45.0 mm
Burr, Egg-shaped with J-Latch Coupling, dia 7.0 mm to 8.0 mm, Head Length 4.8 mm to 11.0
mm, Total Length 28.0 mm to 45.0 mm
Burr, Conical with J-Latch Coupling, dia 5.0 mm to 6.0 mm, Head Length 8.3 mm to 9.7 mm,
Total Length 23.0 mm to 45.0 mm
Burr, Pear Shaped with J-Latch Coupling, dia 5.0 mm to 6.0 mm, Head Length 8.3 mm to 9.7 mm,
Total Length 23.0 mm to 45.0 mm
Burr, Tapered fissure with J-Latch Coupling, dia 1.0-2.1 mm to 1.6-3.2 mm, Head Length 11.3
mm to 12.0 mm, Total Length 31 mm to 45.0 mm
Burr, Circular with J-Latch Coupling, dia 8.0 mm to 15.0 mm, Head Length 0.8 mm to 1.0 mm,
Total Length 28.0 mm
Lindemann Reamer with J- Latch Coupling, dia 2.0-2.3mm, head Length 35.o mm,Total Length
53.0
Physical demonstration should be made available.
Q-1(305)M&E/09
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------2 no
-------------2 no
-------------2 no
-------------4 no
-------------4 no
-------------4 no
-------------4 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no
-------------1 no (ton)
-------------1 no each
-------------1 no each
-------------1 no
Q-1(306)M&E/09
The stretcher should have full length radio-lucent resin hard top / surface.
Two section platform and length from 200cms to 220 cms.
Should have x-ray cassette holder &tray which slides throughout whole length &
side cassette loading facility and accommodates all standard size x- ray cassettes
with close proximity of the cassette to the stretcher for optimal quality.
Hydraulic/ electric height adjustment from 60 cms to 110 cms including mattress,
should allow the use of c-arm and x-ray & high / low position.
The mattress made of high density foam and mattress should be waterproof.
Should have foldable side bars( both side), foldable IV stand, monitor and document
support, bowl holder with support, ancrage /urine bag support, folding push bar,
integrated pop-up push handles, arm rest, oxygen cylinder holder, sliding clamps,
two additional batteries, transformer for battery charger& fixed battery recharging
station.
Hydraulic/electric trendelenburg (foot- end) and reverse trendelenburg tilting.
Stretcher should be epoxy grey polyester coated steel frame.
Four castors with central blocking system, two directional head end pedal control at
each corner & 5th steering castor, four shock absorbers.
Folding telescopic IV pole with two hooks with adjustable height from 50 cms to
125 cms.
Should have 200 kg patient weight capacity.
Should have head immobiliser.
PHYSICAL DEMONSTRATION SHOULD BE MADE AVAILABLE.
Q-1(307)M&E/09
60 kg.
12 kg.
Correct force in case of Lumber Vertebral Column Traction Due to the Roll Section.
COUCH should be of regged metal frame with padding material and dimensions should
be at least: 1900 mm (L), 720 mm (W) & 650 mm (H), COUCH should be such that both
the Microwave Therapy and the Traction Unit are attachable to the same COUCH;and
simultaneously the treatment of two therapies can be given to a patient for cumulative
benefit.
Comprehansive Warranty for one Year
Physical demonstration should be made available
Q-1(308)M&E/09
TECHNICAL SPECIFICATION
CONTINUOUS PASSIVE MOTION UNIT
Electronic Rehabilitator for passive Exercises of the lower limb ensures rapid post operative
recovery.
The unit should have got digital keyboard with LCD display.
Knee and Hip mobilization
Ankle Mobilization is must in the same unit.
Use of Memory Card
Speed during Flexion / Extension Control
Force control
Work time control
Automatic increase in Extension range
Pause during flexion / Extension
Automatic increase in Flexion range
Warm up Cycles.
The unit should have got functional panel on the unit only, but not on the patient stop switch or
remote control for patient safety.
Knee movement breadth : 0 -110
Ankle movement breadth ( mid limb ) : 10 - 70
Speed : 0.8 / sec 4.6 /sec
Force : 0-40 kg
Power supply: 85 -260 V /50-60 Hz
Electrical safety: Class 1 B Standard EN 60601 -1
Physical demonstration should be made available
Q-1(309)M&E/09
TECHNICAL SPECIFICATION
CONTINIOUS PASSIVVE MOTION MACHINE (UPPER LIMB)
The unit should have the following features:
Useful to prevent joint stiffness in the shoulder, post operative recovery of ROM
Should be used for bed side patients on supine position.
The machine is based on casters wheel for easy transportation not on the chair based.
Elevation in flexion range: 0 -180
Elevation in abduction: Complete physiological range
Internal external rotation range: 90 -0 -90
Speed, Range of movement: adjustment by electromechanical limit switch
Arm support for rotating movement.
Input: 12 V DC /50/60 Hz -4.8 W
Output: 12 V DC- 1.25 A
Electric safety : Class II B Standard EN 60601-1
Electromagnetic compatibility : Group 1 Class B Standard EN 60601-1-2
Q-1(310)M&E/09
TECHNICAL SPECIFICATION
COMPUTERISED CERVICAL AND LUMBER TRACTION UNIT
The Traction Unit should have got Seven different traction program modes
Should have High force setting from 2 -100 Kgs.
Should have Low force setting from 0 -98 Kgs.
Should Have Constant LED display of high and low force setting
The unit has got a Self checking and diagnostic facility
Treatment time from 0 -99 minutes
The unit should have got an audible alarm and force release facility at the completion of
treatment time.
The unit should have got a Patient safety switch with force release and audible alarm Hold and
rest time of 0 60 seconds
The unit should have got Battery back up in event of power failure.
The unit should be supplied with the Electric Variable Height Traction Couch (Imported) of
the following specifications:
Positive / Negative head section with breathing hole and pulg
Hand of Footswitch height control
Friction free rolling top
Floor level adjuster
Adjustable angle backrest
Physical demonstration should be made available
Q-1(311)M&E/09
Q-1(312)M&E/09
Q-1(313)M&E/09
6. should periodically reevaluate each patients refill time and automatically adjust for
changes in body position.
7. Physical demonstration should be made available.
Q-1(314)M&E/09
Q-1(315)M&E/09
Q-1(316)M&E/09
High resolution integrated monitor 9/12 with tilt with swivel facilty
256 level of grey scale
Alpha numeric key board with illuminated function. key and status display with panel switched
and foot control.
Should have real time zooming facility dynamic range enlargement and freeze facility.
Should be portable/have handle for transporting machine/should have integrated trolley which is
light weight fitted with wheels which can be easily locked .
Complete software for gynaecology, abdominal viscera & complete obstetric measurements (like
BPD, CRL, FL,AC fetal weight etc) which can be activated be easy one touch access.
The new technology should allow easy and user friendly and special user set up.
Facility for pre and post processing the scans.
Orientation symbol for scan planes, ultrasound probe position with complete display of all scan
parameters.
Multifunction electronic calipers for various measurements with track ball facility for image
magnification and guided biopsy.
Versatile scanner with excellent B and M mode with facility for B+ B and B+M Mode preferably
with cine memory , facility for possible up gradation.
Convex array abdominal transducers of 3.5 MHZ ( preferably multi-frequency probe of 2.7/3.5/5
MHZ), immersible.
Puncture attachments for the above, diameter 1.2 -3.6 mm.
End fire transvaginal probe, multi frequency 5, 6 7.5 MHZ, broad angle of inclination with
puncture attachment for above..
Environment limits
Operating temperature 10 to 40 Deg . VAC
Storage temperature 25 to 70 Deg C
Other accessories like Black & white video thermal printer with 10 rolls of high density recording
paper (may be quoted separately )
Should confirm to CE and IEC or equivalent standards for such category of equipment.
General specification
Of
Office hysteroscope
1. Telescope: Fore oblique 300 telescope, diameter 2 mm, length 26 cm, autoclavable, fiber optic
light transmission incorporated.
Quantity Two
2. Continuous flow Examination sheath (for use with above telescope): An inner and an outer tube
facilitating a continuous flow of distension media, with in and out flow stop cock with lure lock
adaptors, with an outer diameter of 3.6 mm.
Quantity Two
3. Continuous flow operating sheath (for use with above telescope): An inner and an outer tube of
diameter 4.2 mm with channel for 5 Fr. Operating instruments with in and out flow stop cock with
lure lock adaptors.
Quantity Two
4. Semi rigid Operating instruments, 5 Fr.diameter, length of 34 cm, to be used with above
operating sheath:
1. Biopsy and grasping forceps with double action jaws
Quantity Four
2. Scissors pointed with single action jaws
Quantity Four
3. Punch biopsy forceps through-cutting single action jaw
Quantity Four
4. Tenaculum grasping forceps, double action jaws
Quantity Four
5. Palpation probe
Quantity Four
6. Bipolar vaporization electrodes
Quantity Four
5. Video camera monitor and light source:
Endoscopic camera:
single chip camera
700 to 800 lines horizontal resolution
1. The quoted equipment should confirm to CE & IEC standards or equivalent for such
category of equipment
2. The unit should be quoted with all the accessories so that when installed the unit should be
capable of full function without need for additional accessories.
3. The firm or its representative should be based in Delhi for easy after sales repair.
4. 2 years onsite warranty with periodic maintaining visits (minimum 4 visits in a year) over
these 2 years followed by an AMC for the next 5 years.
5. The firm should be willing to demonstrate the equipment if asked for.
Q-1(326)M&E/09
To be used in conjunction with Computerised Sperm Analyser & Its reliability in carrying out
sperm analysis and sperm countingMakler Chamber method of sperm counting with cover slip and
class cover. The makler counting chamber should be 10 microns deep:1/10th of the depth of
ordinary hemocytometers, making it the shallowest of known chambers. Contructed from two
pieces of pitically flat glass, the upper layer serves as a cover glass, with a 1 sq.mm fine grid in the
center subdivided into 100 squares of 0.1 x 0.1 mm each. Spacing is firmly secured by four quartz
pins.
The firm should be willing to demonstrate the equipment if asked for.
10 micron depth
100 X 100 grid
Complete with cover slip
The firm should be willing to demonstrate the equipment if asked for.
Q-1(327)M&E/09
Q-1(329)M&E/09
Q-1(330)M&E/09
Q-1(331)M&E/09
Technical Specification
-For heating of test tubes in removable, autoclavable, anodized aluniminium blocks for
maintenance of required temp with + 2 C, accuracy for ambient to 110C
-Temperature range ambient to 55 C with accuracy + 0.2 C
The firm should be willing to demonstrate the equipment if asked for.
Q-1(333)M&E/09
Q-1(334)M&E/09
For maintaining the temperature of critical biological specimens at desired level during
microscopic observation. An iodized thickness with 50 mm central grove with glass and
175 x 155 mm dimension which should fit on most microscopic stages. Temperature range
ambient to 55C with accurary of + 0.2
The firm should be willing to demonstrate the equipment if asked for.
Q-1(335)M&E/09
Fridge Thermometer
Technical Spefcification
-Medical grade thermometer for calibrating
-Show temp & Humidity
-Work on battery
-Portable can be placed anywhere
-Show Min/Max Temp
The firm should be willing to demonstrate the equipment if asked for.
Q-1(337)M&E/09
-Gamma irradiated endotoxin tested flexible unbreakable, mouse embryo tested glass made
-of following sizes 135u, 150u, 175u
The firm should be willing to demonstrate the equipment if asked for.
Q-1(340)M&E/09
change the filter at the appropriate time. It shouldl have filter alarm with automatic visual
indication.
The firm should be willing to demonstrate
Q-1(344)M&E/09
Q-1(348)M&E/09
Q-1(349)M&E/09
SPECIFICATIONS
NON INVASIVE CO-OXIMETER
SPECIFICATIONS :
VIDEO BRONCHOSCOPE (Adult Therapeutic) :
* Light weight & fully immersible in disinfection solution.
* 3 or 4 nos. programmable remote switches for user's convenience.
* Compatible with semi automatic leakage tester with air flow regulation from
attached light source airpump.
* Compatible with electrosurgical accessories and laser (Nd:YAG, Diode)
Field of View
Depth of field
Insertion tube Dia.
Working Length
Min. Visible distance
Instrument Channel Dia.
Bending Range
:
:
:
:
:
:
:
Standard set should include Reusable & autoclavable Biopsy forceps (Standand) 1no,
Cytology Brush set (5-6 pieces, disposable type), Cleaning and maintenance kit,
Otherwise to be quoted separately.
Standard set should include Reusable & autoclavable Biopsy forceps (Aligator jaws)
1no, Cytology Brush set (5-6 pieces, disposable type), Cleaning and maintenance kit,
Otherwise to be quoted separately.
Q-1(352)M&E/09
Specifications of Adult High Frequency Oscillation Ventilator ( HFOV )
Electrically Powered, Electronically Controlled High Frequency Ventilator for entire range of
Patients > 35 kgs with following important specifications :Frequency
Bias Flow
Mean Air way Pressure
Amplitude
% Insp. Time
:
:
:
:
:
3~15 Hz (180-900bpm)
0 ~ 60 LPM
5~ 55 cm H2O
7- 130 cm H2O
30 ~ 50%
Q-1(353)M&E/09
17. Facility of manual breath, SIGH, inspiratory & expiratory hold, Volume Limit,
18. Bias flow, inspiratory rise settings & Synchronized Nebuliser.
19. Should have Automatic Tube Compensation & Leak Compensation.
Q-1(354)M&E/09
SPECIFICATION
BODY PLETHYSMOGRAPH SYSTEM WITH DIFFUSION STUDY
1) A Single combined fully automatic computerized unit for the measurement of following
parameters :
*
*
*
*
*
*
*
*
2) Body Plethysmograph System with 890 Litres Box with rugged construction of
Aluminum and Security Glass having good thermal conductivity. Should have
Visibility from all directions (from inside as well as from outside).
3) Door construction should be specially designed to provide full proof tightness.
Should have facility for door closing and opening both by Operator and Patient.
4) System has quick thermal equilibrium. Intercom System to be provided for
Communication with patient while sitting inside the Box.
5) Should have Patient friendly Mouthpiece Assembly with facility for easy cleaning
& sterilization.
6) Should Incorporate Precision Quality Pressure Transducer for Box, Mouth
and Flow.
7) Should incorporate heated Pneumotach Transducer for measurement of Flow
& Volume parameters with highest accuracy, reliability & reproducibility.
* Minimum Flow Range : 0 14 Lit/sec (Linear)
* Resistance : 0.5cm H2O/L/Sec.
* Relative Accuracy : < 3%
(Should Meet Criteria for ATS Standards).
8) Provision of Automated Calibration and Test Procedure with Computer.
Each Test can be reviewed/computed on Screen.
9) System should incorporate Integrated Electronic Barometer.
10) Automatic Dosimeter /Nebulizer for Broncho Provocation Test.
(contd. Pg. 2)
Page : 2
11) Diffusion Module should incorporate Linear Gas Analyzers :
* Helium Analyzer, Range 0-15% He, Accuracy + 0.15%
* Carbon Monoxide Analyzer, Range 0-0.350% CO, Accuracy +/- 0.15%.
12) The System should be supplied with Powerful Software & Interpretation with
following features :a) Technique independent testing Patient can inspire or expire without loss of data.
b) Window XP based,
c) Calibration with 3 Litre Precision Syringe,
d) Incentive Spirometry : Flexible Screens which can be enlarged any moment.
e) Flow Volume Loops.
13) Control & measurement of the System should be from PC with following minimum
Specifications :
Pentium IV Core 2 Duo Processor, 1 GB RAM,
Full Keyboard, 17 TFT Colour Monitor,
Mouse, Windows, DVD R/W,
Hard Disc Drive (250 GByte)
HP Deskjet Colour Printer
UPS 1 KVA,
12) The System should have complete Computerized Gas Calibration & Box Calibration.
13) Predicted Equipment of various authors & user definable Predicted to be
incorporated. Facility to Enter & design user defined predicted equation.
14) Reports : Should have many report formats as well as user defined reports with
Editing and Cut/Paste Facility.
15) Lung Volume Colour Bar Graph Printout.
16) Meets all International Safety Standards, CE & ISO.
17) The System should be supplied with following accessories/Goods.
A) Gases :
Diffusion Gas Mixture Cylinder (CO & He) 2 Nos.
B) Accessories :
a) Pneumotach Screens (10 Nos)
b) Pulmonary Filters (100 Nos),
c) Noseclips (10 Nos)
d) Expired Bags (5 Nos),
e) Disposable Mouthpieces (500 Nos).
Q-1(355)M&E/09
SPECIFICATIONS
NITRIC OXIDE MEASURING SYSEM (IN EXHALED AIR)
* For the measurement of :
* Should incorporate easy to use Non-Invasive technique with low operating cost.
* Should Incorporates Piezo Resistance Pressure Transducer for :a) Expired Flow Rate Measurement with
Flow Range : 0.01 to 1 Litre/Sec.
Expired Flow Rate controlled Range : 50 to 350 ml/sec.
b) Expired Pressure Measurement with :
Measuring Range : + 50cm H2O.
Expired Pressure Range : 10 20 cm H2O.
* Should Incorporate NO Analyzer :
i) Measurement Range : 1 to 300 ppb (Bronchial)
ii) Response Time : 25 sec.
iii) Analysis Time : 35 Sec.
iv) Accuracy
: Better than 2.5 PPB
v) Linearity
: error < 0.5 %
vi) Reproducibility : + 2.5 PPB.
* Should Incorporates facility for : * Adjustable Washout and sample Volume.
* Automatic Compensation of drift due to Temperature variation.
* Full quality control & history of Calibration.
* Facility for Serial History Table, Interpretation & report editor Module in the software.
* Should Meet ERS/ATS Standards of measurement.
Should be Supplied with Interface for Computer, Software, Standard accessories & Manual.
Should be supplied with Computer Pentium IV Duo Core 2 Processor, 1 GB RAM, 17 TFT Colour Monitor,
Keyboard, Mouse, Windows, DVD R/W, USB Ports, Hard Disc Drive (1x 250GByte) & HP Deskjet Printer.
Additional Accessories :
* Chemical Absorption Column (5 Nos),
* Pulmonary Filters (100 Nos),
Q-1(356)M&E/09
SPECIFICATIONS
PFT SYSTEM WITH DIFFUSION STUDY
Q-1(357)M&E/09
SPECIFICATIONS
(FOR EXERCISE TEST SYSTEM)
Q-1(358)M&E/09
: 4-20cm of H2O
3. Rate : 4 to 40 BPM.
4. Inspiratory Time : 0.5 to 3.0 sec. with resolution of 0.1 sec.
5. IPAP Rise Time
6. Oxygen Conc.
SPECIFICATIONS
FIBRE-OPTIC LARYNGOSCOPE
SPECIFICATION
Fibre optic Laryngoscope compatible with fibre illuminated (ISO 7376-3) handles
Should have replaceable fibre-optic bundle
Should have variety of blades Macintosh (4 Sizes) & Miller (6 Sizes)
Cold, Bright light 2800 LUX
Detachable & Autoclavable, Stainless Steel Blades
ISO 9001 & CE Standard
Q-1(360)M&E/09
Display
Must be a Color TFT of size not less than 17 inches.
Commonly used buttons must be available for direct initiation e.g. NIBP, Silence Alarm
etc.
Configurable Screen formats such as but not limited to include : View BED, Oxy CRG,
Large Fonts with waveforms, 6, 8 or 10 waveforms display in a single screen, 12 lead
ECG only display, waveforms with minitrends display etc.
Alarm light indicator must be visible from distance and distinguable with type of color
and flashing frequency.
Module to be included
Standard 12 Lead ECG, Masimo SET SpO2, Dual Temp, Respiration, NIBP, 2 ch IBP,
Microstream ETCO2 & Cardiac output complete with one set of Pediatric and adults
accessories each.
IBP must be upgradable to atleast 4 channel
MINIMUM of 4 slots must be available for modules to expand the monitor functions.
3
Essential Features
5
6
Calculations screen for DRUG dose with titration tables must be included.
Facility to freeze the waveforms
Facility to select the alarms levels for various parameters
Should have arrhythmia detection and arrhythmia alarm facility
ST segment analysis.
NIBP modes must include manual and automatic with a choice to select the interval of
automatic readings aset between 1 Minute to 3 Hours
Should have non-volatile trending facility for at least 24 ~72 hours
USB ports must be available to connect additional mouse or keyboard for enhanced
performance.
Should be connectable to central nursing station.
Must have facility to interface with an external slave monitor
Accessories
Other than the one set of accessories included above for adults/paed patients, please
quote separate prices for neonatal accessories.
User's replaceable Recharge Batteries - 2 nos Lithium Ion or better technology must
be included.
Monitor should be supplied with a monitor bracket and necessary hardware for
mounting on a head wall unit.
3 or 4 channel printer module must be included.
Must conform to CE Mark and US FDA standards.
Quote separate prices for following Modules/facility:
Dual channel invasive pressure module
Respiratory Mechanics
Touch Screen operation
Q-1(361)M&E/09
Monitors should have modular design, i.e. one module for every parameter. Modules should be
insertable in any slot without any restriction. Modules should be colour coded to avoid inserting
wrong cables, leads.
2.
Display shall be multi-coloured, display size should be atleast 15" diagonal flat screen high
resolution display and display atleast eight waveforms, positioning of waveforms should be
anywhere on screen.
3.
Should have slave display size 21", should operate independently of main display i.e. waveforms in
slave display are independent of main display.
4.
Display should have two sections, one section shall provide all waveforms as normally displayed,
other section shall provide all numerics, alarm limit and 30 minute trend of each parameter
simultaneously.
5.
Display shall permit viewing of any prameter waveform and numerics from any bed on the system
via manual selection by the users. The function shall not interrupt normal monitoring of
physiological waveforms/values and alarms at the local bed and shall display any one trace from
another bed.
6.
7.
Should include hemodynamics calculations and vital sign and graphic trends. Trends should be
automatically stored for atleast 24 hours in at least one minute intervals.
8.
Numeric monitored data shall be viewable and recordable in a patient chart type format in at
periodic interval.
9.
5 years warranty with 3 years free service with spares and 2 years without spares.
ECG/Resp. 2 modules atleast three leads of selectable ECG should be displayed simultaneously.
Should have option for displaying 12 lead ECG through 5 lead ECG cable. Should include 5 lead ECG
cable.
Invasive Blood Pressure module should have selectable label capability with systolic, diastolic and
mean pressures being displayed 6 modules with reusable pressure transducer.
Non Invasive Blood Pressure - 2 modules. Interval for measurement should be programmeable by user,
manual measurements should also be possible. Should also include adult, small adult, peadiatric and
neonate cuffs.
Pulse Oximetry 2 modules - should provide oxygen saturation percentage level, include adult probe 4
units paediatric probe - 2 units, neonatal probe 2 units.
Cardiac Output 2 modules should also have option for continuous cardiac output.
Temperature - 4 modules.
Q-1(362)M&E/09
1.
2.
Printer- Matrix printer compatible with the system i.e., Gamma Counter, should be
provided for output of measured results.
Power: 220-230V AC, 50HZ
Power conditioning: Uninterrupted power supply (UPS) of reputed firm for the whole
system with maintenance free batteries of reputed make, having at least 30min back-up
time.
Supporting documentation should include Operator manual containing a basic
description of system operation, a detailed description of utility soft wares and
calibration and adjustment procedures.
At least two long half life radioactive sources should be provided for performing quality
control procedures of this system
Maintenance:
The guaranteed up-time of the system within a normal working week, excluding any
planned preventive maintenance, provided the system is on a maintenance contract
should be 95% or 346 days (24x7) per year.
The supplier must ensure availability of expertise service and maintenance at New Delhi.
Spares availability and repair for the next 10years must be assured.
If the specified uptime mentioned above at 8.1 is not achieved, the warranty period will
be extended by double the number of days for which guaranteed up-time criteria was not
met.
Training: On site training for a period of one week should be organized at the time of
installation and for one week after 2-3months of installation. At the same time quality
control of the equipment will be done.
Warranty: Five years comprehensive warranty for the whole system with spares
including well detectors (including crystal), computer system, printer and UPS. The
comprehensive warranty will include regular preventive maintenance of the equipment.
The company should quote Comprehensive Maintenance Contract (CMC) Price
including spares for another 5years.
3.
4.
5.
6.
7.
8.
8.1
8.2
8.3
9.
10.
Q-1(363)M&E/09
Should have Extensive QC feature, like files for X bar on LJ plot available, One file for X
bar M. provide Delta checks available for cumulative review and an option for online QC.
Firm must have its own Calibrators, Controls and reagents for the Analyzer. They should
also provide calibration certificate.
The analyzer should have five years warranty, Reasonable price of AMC to be given after
warranty period.
Should have good installation base in Govt. Hospitals in Delhi and be backed by high
quality support at reasonable cost and unmatched network of well trained service and
application support staff within NCT of Delhi.
The Analyzer should be supplied with UPS of 30 minutes back up.
Should supply standard Blood Mixer along with Analyzer.
The system should be supplied with free reagents of 1000 samples including reticulocyte
count and one complete set of calibrators.
5 years comprehensive warranty.
Free installation at user site.
Standard accessories as per catalogue.
Suitable UPS.
FDA and CE Certification.
Working manual.
Should have authorized service centre in New Delhi/ Delhi.
Equipment should be complete in all aspects to start working from day one.
Q-1(365)M&E/09
4-
56789101112131415161718192021-
In built facilities to identify and temperature deviation beyond alarm set point to
show the error that has occurred and to display, it has been corrected.
Cooling: it should have:- CFC free refrigerants.
- Co2 Emergency cooling system.
- Washable condenser filter and indicator for advising removal/ cleaning of filters.
- In the event of power failular temperature should not drop to below- 10 degree
Centigrade take around 14-15 hours.
- Noise emission< 56 dB.
Cabinet insulated in Polyurethane CFC Free.
LCD display with a resolution of 0.1C.
Panel Control with constant indicating of temperature. Temperature sensor put-on into
liquid medium balanced bottle, simulating the blood temperature.
Alarm test.
Seven day temperature recording thermometer 6 chart, with battery backup (optional).
Power failure, door ajar alarm.
Audible- visible alarm high and low set points. Alarm silent button for audible alarm with
automatic re- connection.
Over side aluminum/ finned copper refrigeration coils provide rapid cool down and tight
temperature control ( + - 1C ) at any set point over the 2-10C range with forced inner
air circulation for maintenance of homogeneous temperature in all sectors.
Interior fluorescent light.
High / low voltage protector.
Mounted on wheels with brake system.
Inner chamber should be corrosion resistant and made up of stainless steel.
It should have ultra thin vacuum insulation with 5 year guarantee.
5 years warranty on compressor and to provide gases for 5 years free to cost and 24
months. Comprehensive warranty on equipment.
Firm to supply one pair of cryogloves along with the equipment.
Electrical connection 220 voltz = 50 HZ.
Company should provide 2 KVA voltage stabilizers.
Q-1(366)M&E/09
GENERAL SPECIFICATION
Tender No.
Equipments Name :
Haemodialysis Machine
Q-1(367)M&E/09
Q-1(368)M&E/09
Essential Accessories:
Main Unit should be supplied with:
One coil Disk applicator.
One set of condenser applicator.
Mobile trolley.
Q-1(370)M&E/09
b) Wave form acquisition, display and Storage: It should have a time base range of 0.2ms/div
to 5 sec/div,selectable for specific tests.
c) Amplifiers : TFT Monitor 17. The display modes of normal, normal and plus/minus with
artifact rejection facility and average display sensitivities 1 microV/div to 10mV/div,
depending on test, input impedance of >100Mohm. The software control for Sensitivity from 1
micro V/ div to 10mV/div, High filters 15Hz to 10kHz and low filters 1 to 500 Hz.
d) Electrical Stimulator: Each channel with current (from 0 to 100mA) and voltage (0 to
minimum 400v) stimulation facility and probe with adjustable intensity, with stimulation
duration of 0.01-1 ms and 0.1-100 per second. Stimulator should have probe for both adult &
pediatric size.
e) Application Software: Software should be based on the Windows XP operating system with
easy to use menus, flexible protocols, Anatomy Browser, with standard settings and user
definable settings software. It should have software packages for doing Quantitative EMG and
facility for EMG Free Run Storage on hard drive, along with audio with Replay. Facility for EMG
is desirable.
Software packages for Monitor Nerve Conduction, Sensory Nerve Conduction,
F-Wave, H-Wave and blink reflex studies.
All the test results data should be incorporated into Microsoft Word Software for patient
reporting.
f) Reusable accessories and required consumable including the following for performing all the
above studies should be included.
1.
2.
3.
4.
Q-1(371)M&E/09
Q-1(372)M&E/09
There should be sterilization cycle for both bagged and not bagged tools including a
fast cycle at 1340 C &1210 C. the sterilization time and the drying time should be
combined and automatic.
There should be rapid warm up facility. All WARM up, sterilization and drying
cycles should be completely automatic and all parameters should be microprocessor
controlled.
There should be a motor for water charge. The heating element should be placed at out
side of the sterilizing chamber and should not be in touch with water.
The system should be supplied with incubator for biological validation as standard
configuration of the same manufacturer.
Optional printer.
The system should comply with International standards for sterilization and should be C. E
marked manufactured by I S O certified company.
Q-1(373)M&E/09
Specifications of Tonopen
1. Portable / Handheld
2. IOP range 5 to 50 mm Hg.
3. Provide averaged readings on LCD display screen
4. Power source : long life battery power or
rechargeable battery
5. Supply of batteries for one year
6. Warranty
7. Transducer- 1-1.5mm, microstrain gaze
8. Accessaries: ocufilm tip covers
Q-1(375)M&E/09
2.
3.
4.
5.
Anti-reflective coating
Holding ring sizeTwo small size & Two large size ring
Material- CR 39
For slit lamp biomicroscopy
ANNEXURE C
SPECIFICATIONS
+ 78 D DIAGNOSTIC LENS FOR FUNDUS EXAMINATION
1.
2.
3.
4.
5.
Aspheric lens
Anti-reflective coating
Holding ring sizeTwo small size & Two large size ring
Material- CR 39
For slit lamp biomicroscopy
Q-1(376)M&E/09
1. Imported
2. With 5.5 gm, 7.5 gm and 10.gm weights
3. Test block
4. Conversion table
Q-1(377)M&E/09
Q-1(378)M&E/09
Contact dia.
Static FOV.
Style
1.47 X
19 mm
160 degree
Large
1.5X
18mm
160 degree
Medium
1.55X
17mm
160 degree
Small
Image magnification
Laser spot
magnification
Contact dia.
16.5mm
1.6X
0.63 X
15mm
Lens Height
Image magnification
Laser spot
magnification
Contact Dia.
Static FOV
32.2 mm
.93X
1.08X
18mm
150 degree
Q-1(379)M&E/09
14-40mm
5-10 mm
5. Formula for IOL computation SRK 1, SRK II, T Holladay, Hofler Q Haigis
6. Instrument table
7. Printer
Q-1(380)M&E/09
separate battery charger with main cable, 230V Mobile on four double castors with cap, central
brake and spring-loaded directional castor to be activated by foot pedal. The table should be
quoted with standard with all standard accessories.
TECHNICAL DATA
Overall length, two head plate
Overall length, with head plate
Width of table top
Total width
Base (L x W)
Daim of swivel castors
Height adjustment
Trendelendurg
Reverse trendelendurg
Lateral either side
Back section
Leg plate divided
Swiveling of leg plate
Head section
Tilt of head section pad
:
:
:
:
:
:
:
:
:
:
:
:
:
:
:
1780mm
2130mm
540mm
590mm
1120 x 580mm
125mm
from 720 1080mm
30 deg.
30 deg.
+/- 20 deg.
+ 70 / -50 deg.
+20 / -90 deg.
55 deg.
+ 25 / -45 deg.
25 deg.
STANDARD ACCESSORIES
Shaped head rest,, connecting piece, Universal adaptor, shoulder plate, leg section, arm rest, body
restraint strap, anesthetic frame, anesthetic frame extension, infusion pole, body restraint strap. If
any other essential accessories should also be quoted.
Q-1(381)M&E/09
A-Scan can be used for biometric calculation and for quantifying the
reflectivity of lesions in the eye and orbit.
B-Scan is used for imaging the anatomy.
System completes with all hardware and software and report printer and
image recorder is required:
Technical Specification:
1.A-scan mode
2.B-scan mode
3.Dynamic movie archiving
4.Laser & video CD recording facility
5.Auto & manual measure function
6.Distance & area measurement on B-scan images
7.Vector A-scan measurement
8.Simultaneous B-scan with vector A-scan
9. A-scan dynamic recording with gain adjustments
10 Facility for IOL power calculations(all formulas)
11. Accessories & Spares:
System as specified
A Scan Probe-01; frequency > 10 MHz
B Scan Probe-01; frequency> 10 MHz
Integrated or compatible recorders/printersCD Recorder
Report printer
12. The unit shall be capable of being stored continuously in ambient
temperature of 0-50deg C and relative humidity of 15-90%
The unit shall be capable of operating in ambient temperature of 20-30 deg
C and relative humidity of less than 70%
13. Power input to be 220-240VAC, 50Hz fitted with Indian plug
Reset table over current breaker shall be fitted for protection
Voltage corrector/stabilizer of appropriate ratings meeting ISI
7.
8.
9.
10.
11.
12
13.
14
15.
16.
Q-1(383)M&E/09
SPECIFICATIONS OF GONIOSCOPES
THREE MIRROR GONIOSOPES
(GOLDMAN TYPE)
1
2
3
4
Anti-reflective coating
Angles of Mirrors590, 670, 730
Universal style
Lens height 30-33 mm
SINGLEMIRROR GONIOSOPES
(GOLDMAN TYPE)
1. Anti-reflective coating
2. Angle of Mirror 620
3. Does not require methylcellulose for gonioscopy
Anti-reflective coating
Angles of Mirrors640
Ergonomic handle to hold the lens
Small diameter contact surface
Does not require Methyl cellulose for gonioscopy
Q-1(384)M&E/09
Q-1(388)M&E/09
Q-1(389)M&E/09
Q-1(390)M&E/09
25-30o
Hopkins-II lens
Adult percutaneous nephroscope sheath 20.8Fr
Stone grasping forcep 3.5mm diameter
Adult percutaneous nephroscope outer cover 24 Fr
Telescopic metallic dilator 9-30Fr with guide rod
Amplataz facial dilator set 30Fr, 26 Fr
Alligator jaw forcep 5Fr
24Fr inner resectoscope sheath with oblique beak
2
1
4
1
1
2 each
2
2
Q-1(391)M&E/09
Qty
(nos.)
1
Q-1(392)M&E/09
Q-1(393)M&E/09
Q-1(394)M&E/09
h. Pipes and fittings should be of SS & bronze fitted with ball type & solenoid valve
i. The sterilizer should be complete with a water ring vacuum pump.
j. The autoclave should be fully programmable with PLC based technology to control
&monitor different sterilizing cycles depending upon the load. P.L.C. should be of 4 Line
display (80 characters) displaying Date, Time, Pressure Temperature & Status of the load.
k. P.L.C. should be of visible display displaying Date, Time, Pressure Temperature & status of
the load. The manual operation facility is provided as a stand by control.
l. The autoclave should be equipped with a printer to record & Print the information during the
cycle such as temperature, pressure, cycle time etc.
m. A rotary witch should be provided for operating cycle in manual mode in case of P.L.C.
failure.
n. Automatic system for operating sterilizer, controlled with Air break contactors, Pressure
switch , Solenoid Valves with electronic power supply. The unit can also be operated
manually.
o. Electrical steam generator and Boiler plate made of Stainless Steel and gauge glass tube with
protector for viewing of water level.
p. Air Over steam pulsing pressure system.
q. Automatic high pressure water feeding pump.
r. Safety valves, Self sterilizing vacuum drier, Pressure gauge, Compound gauge, Steam trap,
Swing Check Valve & Screen Plug.
s. The sterilizer should be complete with a water ring vacuum pump.
t. Equipment should have warranty of 2 years and AMC for 4 years & CMC for next 4 years
u. Tenderer should have an minimum experience of 5 years of maintenance of these type of
equipment.
Q-1(395)M&E/09
Screen 36 cm HR tube.
It should be compatible with S-VHS, RGB
It should have built in speaker system.
There should be Y/C signal socket.
It should also be RGB signals.
Dimensions : 346 mm x 340mm x 430 mm (wxhxd) (Approx.)
Endovision Camera
Endovision single chip cemera with IPM (Integrated Image processing module). Focal
Length should be 25 mm-50mm. It should have high horizontal image resolution more than 250
lines and also should integrate parfocal zoom lens. It should have 2 programmable function key in
the camera head for control of cemera function, video, printer/recorder function. It should have
automatic white balance with memory function. It should have alternatively manual or automatic
digital exposure control, weight of control unit 2.95 kg (approx), power supply 100-240 VAC,
50/60 Hz. It should be supplied with following accessories:BNC connecting cables, S-SHS connecting cable, RGB sync connecting cable, set and
Keyboard for character generator and control of cemera functions or any upgraded recording
system.
Specifications:
Image sensor: CCD chip
Min. sensitivity : 3 lux
Q-1(396)M&E/09
Frequency 50 Hz.
Max. Temperature of T out 43 C +- 1.5* C
Max. Flow 1000 ml/min or better
Alarm limit -+/-1.5*C of set temperature
Set point temperature 30-39 C
Heating and measuring technology infrared
Accuracy of flow meter -+ /- 20%
Compliance Report to be submitted in a tabulated and point wise manner
Clearly mentioning the page/para number of original catalogue/date sheet
User list to be provided with performance certificate
Demonstration is a must.
Should have local service facility
Comprehensive Guarantee 2 years & 5 yrs CMC INCLUDING ALL
PARTS.
Q-1(397)M&E/09
Q-1(398)M&E/09
2 each
2 each
Rougeurs
Straight (3 sizes)
Curved (3 sizes)
2 each
2 each
Pituitary forceps
Straight (2 sizes)
Curved (2 sizes)
2 each
2 each
Q-1(400)M&E/09
DEPARTMENT OF RADIOTHERAPY
OPERATION TABLE SPECIFICATIONS
The Operation table should have following features:
1. Four section table top with divided foot section.
2. Table top should be constructed from a high pressure laminate to permit x-ray penetration
and fluoroscopy.
3. All table positioning, i.e. height, back section, lateral tilt, trenelenburg and antitrendelenburg, except foot and head section should be operated hydraulically.
4. Should have a manual position selector whose location should be interchangeable between
foot and head end.
5. The casings on the frame and centre supporting column should be made of hygienic
stainless steel.
6. Mattress should be radioluscent and suitable for fluoroscopy.
7. Accessories should include
8. Measurements:
Q-1(401)M&E/09
The model should have female lower body with removable soft outer skin as well as anatomically
accurate timbrial and ovaries for lecture of uterine sounding,bimanual pelvic examination,
insertion and removal of contraceptive devices.
It should be provided with
1 normal anteverted uterus and transparent top and round ligaments
1 normal uterus
6 uteri with external pathologies
2 normal cervices with patent as for IUD insertion/removal
6 cervices with pathologies
Supplied with talcum powder and carrying bag.
The firm should be willing to demonstrate the equipment if asked for.
Q-1(402)M&E/09
10.The monitor should be capable to support Internet Networking and compatibility to use with
central monitoring system
11. There should be alarm limit setting for every parameter
12.It should have priority color coded audio visual alarm system with bright prompt message on
the screen. There should be a separate color coded audio visual alarm when patient data deviates
from normal limit and machine failure , improper function
13. There should be complete ST segment and arrhythmia analysis
14.The monitor should have OxyCRG screen
15. There should be various calculations like Drug dose, Oxygenation, Ventilation, Renal and
Hemodynamics
16. It should come with dual exchangeable Li-Ion batteries with more than 3 hours battery backup
17.There should be a provision for built in 3 channel thermal recorder
18. There should be hot keys and Icons on buttons and Iconic symbols on touch screen as well
19.The monitor should be FDA,CE marked and ISO approved. The equipment should comply with
IEC 60601 series of standards.
The firm should be willing to demonstrate the equipment if asked for.
Q-1(403)M&E/09
Q-1(404)M&E/09
BOD incubators
Specifications:
Microprocessor controlled
Capacity: 240-250L approx.
Temperature range: 4o C to 80oC
Interior chamber: Adjustable stainless steel shelves for easy cleaning and
decontamination.
Digital display for temperature and time.
Heating by natural convection for homogenous temperature distribution.
Adjustable fan speed
Minimum turbulence
Adjustable safety thermostat for temperature set at 1oC increment
Temperature accuracy + 0.5oC
Internal glass door for observation
Power 220-240 V; 50/60 Hz
CE, Iso 9001, ISO 13485 Marked or equivalent marked.
Q-1(405)M&E/09
19. Cart
20. Sterilization tray for accessories
The above mentioned device should have the following components and specifications.
12. It should be capable of being used for both laparoscopic and open surgery.
13. It should have an ultrasonic generator with fixed frequency of 45.5 55.5 kHz or above
confirming to IEL standards class I CF
14. The instrument should have a minimum of 5 power levels with power level display. The
power output should not be less than 100 Watts (continuous) & 150W (interval). It should
have power entry filters to suppress electromagnetic disturbances and should be
defibrillator protected.
15. It should have vibration range of 50-100 microns.
16. Hand-piece with in-built transducer compatible with 10mm to 5mm instruments and
attached to generator by autoclavable silicon cable.
17. Hand-switch activation adopter for blade & hook probe.
18. The generator must be CF isolated applied device and conforming to IEL safety standards
Class 1, Type CF and Electromagnetic compatibility and Defibrillator protected.
19. The system should have a foot switch with dual level control.
20. The system should have a standby mode, audible indicator with adjustable volume control
for active probe.
21. Should have warning system for worn out probes, broken cables or improper connections.
22. The system should be supplied with mobile cart for ready transportation.
Laparoscopic Instruments
6. Dissecting Hook, 5mm diameter, 33 - 358cm long
7. Curved Blade, 5mm diameter, 32-38cm long
8. Ball coagulator ,5mm, 28 32cm long
9. Laparoscopic Hand Activated Curved Coagulating Shears (LCS)- 5.5 mm diameter,
32-38cm long.
10. Laparoscopic Coagulating Shears, 10mm diameter, 33- 38cm long, capable of working
in three modes flat, blunt and sharp.
Open Surgery Hand Instruments
6. Coagulating Shears, 8.5mm 10mm, 15 - 23cm long, has cylindrical tip blade of length
18 - 20mm, capable of sealing blood vessels up to 5mm in diameter. Instrument should be
hand and foot activated.
7. Curved Coagulating Shears, 5.5 mm shaft diameter, 15 -23cm long, capable of working
in three modes flat, blunt and sharp.
8. Straight coagulating shears, 10 mm shaft diameter, 15 - 23cm long capable of sealing
blood vessels up to 5mm in diameter capable of working in three modes flat, blunt and
sharp.
9. Curved blade with grip, 18- 23cm long.
10. Curved dissecting hook, 5 mm diameter, 18-23 cm long.
The specifications given above are approximate and minor variations without
alteration of function using ultrasonic technology are acceptable.
4 Environmental factors
1. Shall meet IEC-60601-1-2 :2001(Or Equivalent BIS) General Requirements
of Safety for Electromagnetic Compatibility or should comply with 89/366/EEC; EMC-directive.
2. The unit shall be capable of being stored continuously in ambient temperature
of 0 -50 deg C and relative humidity of 15-90%
3. The unit shall be capable of operating continuously in ambient temperature of
10 -40deg C and relative humidity of 15-90%
5 Power Supply
1. Power input to be 220-240VAC, 50Hz fitted with Indian plug
2. UPS of suitable rating with voltage regulation and spike protection for 120
minutes back up.
6 Standards, Safety and Training
1. The generator must be CF isolated applied device and defibrillator protection must be available.
2. Should be FDA, CE, UL or BIS approved product. Manufacturer should have ISO certification
for quality standards.
3. Electrical safety conforms to standards for electrical safety IEC-60601 / IS-13450
4. Comprehensive warranty for 2 years and 5years AMC after warranty.
5. Undertaking from manufacturer to provide after sales service for 10 years after warranty period
is over either directly or through authorized agent should be submitted.
5. Facility for after sales service should be available in Delhi.
6. List of installations in other major institutions in Delhi must be quoted.
Q-1(406)M&E/09
Q-1(407)M&E/09
Q-1(408)M&E/09
NEEDLE HOLDER
S.NO.
1.
2.
SPECIFICATIONS
Castroviejo Micro Needle Holder, flat handle with
ratachet, straight DIAMOND DUST jawas, regular box
lock, 5-3/4/11.5 cm.
(Recommended suture size: 5-0 and smaller)
Jacobson Micro Needle Holder, flat handle with ratachet,
straight DIAMOND DUST jawas, regular box lock, 63/4/17 cm.
(Recommended suture size: 7-0 and smaller)
QTY
2 Nos.
2 Nos.
FORCEPS:
S.NO.
1.
2.
3.
4
5.
6.
7
SPECIFICATIONS
QTY
2 Nos.
Dennis Micro Forceps round handle 1 mm straight
(DIAMOND DUST ring tips 7-1/4/18.5 cm counter
balanced
Micro Forceps light weight round handle 1 mm Debakey 1 Nos.
tips 8-1/4/21
Micro Forceps light weight round handle 1 mm Debakey 1 Nos.
tips 7-1/8/18.1 cm
Dennis Micro Forceps, round handle 1mm Debakey tips
1 Nos.
7
Dennis Micro Forceps, round handle 1mm Debakey tips
1 Nos.
8-1/4/21 Counter balanced
Gerald Forceps, flat handle, 1 mm serrated tips, 7/18 cm 1 Nos.
Gerald Forceps, flat handle,1mm serrated tips, 71 Nos.
3/4/19.5 cm
CONTD.ON 2
SCISSORS:
S.NO.
1.
2.
3.
4.
5
6
7
8
SPECIFICATIONS
Jacobson Micro Scissors, spring style round handle 45
deg angles nano blades, 6-3/4/17 cm
Jacobson Micro Scissors, spring style, round handle 125
deg angled micro fine blades,6-1/2/16.5 cm
Jacobson Micro Scissors, spring style, round handle 25
deg angled micro fine blades, 6-3/4/17 cm
Jacobson Micro Scissors, spring style, round handle 90
deg angled micro fine blades, 6-1/2/16.5 cm
Jacobson Micro Scissors, spring style, round handle 60
deg angled micro fine blades, 6-3/4/17 cm
Jacobson Micro Scissors, spring style, flat handle 45 deg
angled micro fine blades, 6-1/2/1.5 cm
Jacobson Micro Scissors, spring style, flat handle 60 deg
angled fine blades, 6-1/2/16.5 cm
Jacobson Micro Scissors, spring style,flat handle 25 deg
angled fine blades, 6-1/2/16.5 cm
QTY
2 Nos
SPECIFICATIONS
Titanium Lambert-Key Aorta Clamp, 3 cm atraumatic
jaws, 8/20
Titanium Debakey clamp, 10 cm straight jaws, 12/30.5
cm
Titanium Micro Needle Holder ring handle straiaght
DIAMOND DUST jaws, 7-1/4/18.5 cm
QTY
1 Nos.
1 Nos.
1 Nos
1 Nos
1 Nos
1 Nos.
1 Nos.
1 Nos.
CLAMPS:
S.NO.
1.
2.
3.
1 Nos.
1 Nos.
RETRACTORS:
S.NO.
1.
SPECIFICATIONS
Modular I.M.A. etractor with provision to attach
sternumblades or Lateral Thoracic Blades
QTY
1 Nos.
Q-1(409)M&E/09
Description of function
1.1 Cardiac Catherization is most commonly required to do angiography of blocked vessels in
the heart. Flat panel is the latest in digital X-ray imaging technology.
Operational requirements
2.1
Flat Panel Single-Plane Cardiovascular Catherization Laboratory system with Digital
Subtraction Angiography with a Floor/Ceiling mounted arm stand and digital imaging Xray System for Cardiovascular Diagnostic and Interventional Procedures.
Technical Specifications-The model should the latest by a given company. The company should undertake that no newer model has been
produced by it.
3.1
X-RAY TUBE
Focus:Dual
Anode Heat: 1.5 MHU or higher Capacity.
Maximum heat dissipation capacity of at least 150
Oiled or water cooled to ensure continuous operation
Latest generation tube for noiseless operation to support long-term investigational
procedures
3.3
IMAGE ACQUISITION SYSTEM
1 Flat Detector of current generation, Good detector high spatial resolution acquisition and
display in Matrix of at least 1024X1024.
2. Flat Panel detector system with excellent spatial and contrast resolution 20cmX20cm
detector plane(25cm diagonal)with a pixel size greater than 180 um or 30cmX40cm
detector plane(48cm diagonal ) with a pixel size greater than 150 um.
3.Frame rates selectable from7-30 frames per seconds
3.4
Bit or higher
3.6
3.7
3.8
3.9
3.10
3.11
HEMOXIMETER
Hemoximeter for measuring Hb and oxygen saturation during cardiac catheterization
complete with all accessories like rinse solution,calibration solution etc for at least 1 year.
System Configuration Accessories, spares and consumables
4.1
Main Unit C-Arm with Gantry, X-RAY generator and Tube and integrated Flat
panel detector10
4.2
4.3
4.4
4.5
4.6
4.7
4.8
4.9
4.10
4.11
4.12
4.13
4.14
4.15
The system should contains all the above accessories in Integrated or as separate accessories.
Environmental factors
5.1
5.2
5.3
5.4
The unit shall be capable of operating continuously in ambient temperature of 10-40 deg C
and relative humidity of 15-90%
The unit shall be capable of being stored continuously in ambient temperature of 0-50 deg
C and relative humidity of 15-90%
Shall meet IEC-60601-1-2:2001(or Equivalent BIS) General Requirements of Safety for
Electromagnetic Cimpatibility
1.The chosen supplier would be asked to undertake a turnkey Project wherein necessary
civil work modifications like Flas Ceiling, Wall Tiling, Anit Static Flooring and finishing
works would be provided by them under the supervision of the support staff
eg.CPWD(civil)
2. The supplier would also provide the Scrub area and the Catheter wash area.
3. The supplier also would provide the necessary furniture like tables, computer chairs,
cupboards, catheter hand wall mounts etc.
5.5
5.6
1.The Air-conditioning involves 10 Tones of Air Conditioning units and these would be
provided by the supplier and maintained throughout the life of the cath-lab under the
supervision of the support staffs eg CPWD(Air-Conditioning)
2. The entire Cath-Lab including the Air Conditioning should be connected to the
Generator of the hospital.
Proper shielding should have to be done by the supplier to minimize radiation leakage as
per AERB and BARC regulations
Power Supply
6.1
6.2
6.3
6.4
6.5
power input to be 220-240VAC, 50Hz/440 V 3 phase as appropriate fitted with Indian plug
Resettable overcurrent breaker shall be fitted for protection
Suitable Servo controlled Stabilizer/CVT for the entire cath lab
UPS of suitable rating conforming to shall be supplied for computer system
The Power requirements involve laying a 125 KVA Cable from the substation to the CathLab and making a Bus-Bar and a Power Distribution Board and this would be done by the
supplier as a turn key project under the supervision of the support staffs eg.CPWD(Elect)
7.3
7.4
Documentation
8.1
8.2
8.3
8.4
8.5
8.6
Q-1(410)M&E/09
: 2 Channels
: Systolic, diastolic and mean flow
Pulsatility index,insufficiency rate,
Integral and the maximum derivative
Pressure
Calculations
: 2 Channels
: Systolic, diastolic, mean values and the maximum
derivative
Auxiliary channels:
No. of channels
:2
One channel for ECG monitoring and the second channel
For Doppler Probe
2.
3.
4.
5.
6.
A)
B)
C)
D)
E)
F)
G)
H)
I)
Q-1(413)M&E/09
Q-1(415)M&E/09
VIDEO THORACOSCOPE :
*Flexible & deflectable distal tip
*Integral light guide cable
*Latest Colour Chip technology
*Compatible with Laser & Electosurgical accessories
*2-3 remote control switches for better operational control
*Fully immersible in disinfectant solution
*Field of view
:
*Depth of view
*Tip bending range
*Distal end dia.
*Insertion tube dia.
*Instrument channel dia.
Q-1(416)M&E/09
both inspired and expired values. Must include 20 nos each of filter, watertrap,
sampling line and airway adaptor with each module
18. Cardiac Output 1 no modules for each monitor for measurement by thermo
dilution method. Should have REF and PCWP measurement
19. Should have EEG Module 1 modules for each monitor. Minimum 2 channel EEG,
include 1 no. Accessory kit for dual montage configuration with 50 electrodes with
each module
20. Graphical and Numeric monitored data should be recordable. Must include
atleast 3 channel thermal array recorder with each monitor
21. Monitor must have capability to use all modules i.e. ECG/NBP/Spo2/Resp/2 x
temp/2 x IBP/cardiac Output/Co2/EEG/Recorded together simultaneously
22. Include necessary imported wall mount for the monitors
23. Include atleast 30 minutes UPS backup for each Monitor
Q-1(417)M&E/09
8) Electrodermal
response amplifier.
9) GSR
10) Blood flow
SPECIFICATIONS FOR BMR APPARATUS
Description: -
Q-1(418)M&E/09
1.
2.
3.
4.
Q-1(419)M&E/09
Description: Should enable measurement, computation, printout of all Spirometry, Flow Volume
Parameters, Maximum Ventilation Volume, Inspiratory Capacity, Expiratory
Reserve Volume, etc.
System should have Dry Rolling Seal Spirometer (12 Litre Capacity).
Range
Accuracy
:
:
Volume 0 to 12 Litres.
Volume 2%; Low 3%.
Should incorporate less than 0.06 cms H2O/Lsec, for highest accuracy &
reproducibility
Should have in built graded scale for calibration procedure (0-12litres).
Accuracy of measurement should not be effective with Relative Humidity, water &
Saliva droplet.
Should be supplied with USB interface for computer, Operating window Software,
Standard accessories & instructions Manual.
Computer Pentium IV 3.0 GHz or more CPU, 512 RAM, 15 VGA Colour Monitor, CD R/W
Drive, Keyboard, Mouse, Window 2000, Hard Disc Drive (1 80 Gbyte), HP DeskJet Printer, to
be supplied.
Q-1(420)M&E/09
Q-1(421)M&E/09
Q-1(424)M&E/09
Q-1(425)M&E/09
SPECIFICATIONS
RESEARCH MICROSCOPE WITH DIGITAL CAMERA SYSTEM
Quantity required: One
1. Research Microscope with infinity optical system, par focal distance of 60mm/45mm
with magnification range = 40X to 1500X for observation, precentered and refocused 12V
100W illumination built in auto: photo present switch. Sideentopf design trinocular tube
with FOV 22 mm can be upgradable (25 mm FOV), inclined at 25/30 degree angle.
2. Eye piece: 10X eyepieces with diopter adjustment on both the side. Eyepiece tube and
eyepiece should be anti fungal type.
Sextuple nosepiece to accommodate six objectives, coarse fine focusing with 0.1micron
rotation, rectangular stage capacity to hold two specimens at one time. Stage handle and
focusing knob should be controlled with one hand.
3. Condenser: Phase contrast condenser having five or more positions with 3 positions for
phase contrast : 10X,40X,100X, one position for dark field :10X,40X one position for bright
field : 4X to 100X.
4. Fluorescent attachment: Fluorescent attachment 100W with red, blue, green, UV filter.
Preferable narrow band with 100W mercury burner with built in hour meter.
Objectives:
Plan achromat
Plan fluorite
5. Digital camera : 2/3 high density CCD chip, approx, 12million pixels resolutions, and
time lapse facility incorporated within the controlling software of the digital camera,
interface card along with compatible C-mount lens.
6. LCD projector : To project the microscopic image to a full screen on the wall for
teaching purpose only.
7. Compatible computer : Intel Pentium P4, with 2.4GHZ or higher Pentium processor, 60
GB or higher HDD, 512 MB DDR RAM or higher, 1.44MB FDD, 17 high resolution
colour monitor, windows 2000/window XP operating system, optical mouse, 104 keys
keyboard, multimedia kit, UPS for 45 minutes backup.
High resolution colour inkjet printer with 2880 dpi resolution for photo quality image
documentation.
8. Voltage Stabilizer for microscope.
9. Image analysis Software should have following features:
Should be capable of handling a wide variety of CCD Cameras (both Digital &
Analogue) including the 3 chip cooled CCD type.
Full support to 8-12 & 16 bits precision grey scale, 24 bit color and 32 bit floating
point image.
Able to create in focus composite image from partially in focus source image stacks
with EDF (Extended depth of Field (0)
Able to create composite color image from an infinite number of source grayscale
image with the color composite tool Create Fast Fourier Transformation both
forward and inverse transformation.
Should be able to compose and send email messages with the group.
Should be able to build a large image from multiply, smaller location acquisitions
with Stitching and Tiling tools.
Q-1(426)M&E/09
Specification
(Human Skull)
Quantity:
Adult: 50
Complete with detachable skull cap.
Quality: Good
Q-1(427)M&E/09
Specification
(Vertebral coloum)
Quantity: 50 sets
Cervical vertebrae: 50 sets of all seven vertebrae
Thoracic vertebrae: 50 sets of all twelve vertebrae
Lumbar vertebrae: 50 sets of all five vertebrae
Sacrum: 50 nos.
Quality: Good
Q-1(428)M&E/09
4. Control Panel: Contains lighted blower and light switches, solid state speed controller for
motor/blower assembly, controls for UV lights (where applicable), and circuit overload protection.
5. Lighting: Provides 100 foot candles 30" from the fluorescent tubes.
General
1.
Noise Level: Less than 65db on the "A" scale at operator's working position.
2.
Vibration Level: Essentially vibration free at-work surface because work table need not be
coupled to main frame.
Certification: All units factory leak checked and certified before shipment using calibrated
DOP photometer and generator.
3.
4.
Q-1(429)M&E/09
b)
d)
5. Prosthetic kit
Q-1(430)M&E/09
Q-1(431)M&E/09
Q-1(432)M&E/09
Flame Photometer
Description of Function: It is used exclusively in the quantitative determination of metals in solution,
especially alkali and alkaline earth in the given samples. Qualitative determination is also possible as each
Q-1(433)M&E/09
Q-1(434)M&E/09
SPECIFICATIONS
MAGNIFICATION
OPTICAL SYSTEM
EYE PIECE
fungal
NOSE PIECE
OBJECTIVE
FOCUSING SYSTEM
STAGE
ILLUMINATION
PHOTO SWITCH
CONDENSER
OTHERS
BINOCULAR MICROSCOPE
Quantity required: 50
1. Microscope - Should have stand with all glass high quality coated optics and cast
aluminum body.
2. Eyepiece - 10X (Pair) with high eye point and eye guards with adjustable interpupillary
distance (54 74mm).
3. Eyepiece tube- Binocular eyepiece tube, 45 angle.
4. Nosepiece 4 position, revolving nosepiece with backward tilt.
5. Objective plan achromatic objective 4X, 10x, 40X, 100X oil immersion.
6. Illumination- should have the option for halogen 30Watt or LED illumination.
7. Stage Gear based XY stage movement, with right hand control and front loading.
8. Focusing smooth coarse and fine adjustment knobs.
9. Condenser condenser 0.9/1.25 with diaphragm aperture and filter.
10. Antifungal all optical parts should be treated with antifungal coating.
11. Filter: built in blue filter.
12. Warranty- 3 years.
13. Guaranty- 2 years.
Q-1(436)M&E/09
Q-1(437)M&E/09
4.
5.
6.
7.
8.
Q-1(438)M&E/09
Q-1(439)M&E/09
3.
It should be able to perform accurate and consistent detection of HIV RNA, HCV RNA
and HBV DNA in donor plasma through NAT method of Transcription Mediated Amplification
(TMA) technique.
4.
System should be able to do Discriminatory tests for HIV, HCV and HBV reactivity using
the same platform and similar or same reagents as the multiplex assay.
5.
System should have throughput of minimum 100 or more Individual. Donor Tests
to be processed within 6-7 hours using one system.
6.
It should use Single Tube Technology from start to finish minimize sample
and sample transfer.
handling
7.
Should have an internal control to be added to each reaction tube in the very first step of
the assay to ensure assay integrity.
8.
The requisite test kit should consist of ready-to-use reagents and chemicals
necessary for the whole NAT procedure.
9.
The Amplification in the testing process should not be inhabited by anti
heparin.
10.
coagulants or
Should have Analytical sensitivity equivalent or better than (95% Detection Limit
for routine testing).
11.
Requisite no of computers for the testing system should be provided with printers and
UPS.
12.
All essential accessories as pipettes, Electronic pipette, centrifuge machine, timer and
barcode scanner and barcode printer of desired specifications for the
functioning of the
machine should be provided as part of the system.
13.
All reagents to be supplied with the system till the equipments is standardized and
calibrated for its effective performance.
14.
15.
16.
All the rates for the consumables and reagents should be provided.
The NAT system must be a proven one with a strong service base in India.
17.
The unit shall be capable of being stored continuously in ambient temperature of 0-50 deg
C and relative humidity of 15-90%.
18.
The unit shall be capable of operating continuously in ambient temperature of 10- 40 deg C
and relative humidity of 15-90%.
19.
20.
Voltage corrector/stabilizer of appropriate ratings meeting ISI Specifications
(Input
160-260 V and output 220-240 V and 50Hz) UPS of suitable rating shall be
supplied for
minimum 1 hour backup for the entire system.
21.
22.
Comprehensive warranty for 2 years and 5 years CMC after warranty with rates.
23.
Comprehensive training for lab staff support services till familiarity with the
system.
24.
25.
list.
Log book with instruction for daily, weekly, monthly and quarterly maintenance check
26.
Q-1(440)M&E/09