HAEMODIALYSIS MACHINE

1. General Haemodialysis Machine with reverse osmosis system is essential

eqpt to carry out haemodialysis of renal failure patients.
2. Physical / Tech Characteristics
a. Feature
(1) Hemodialysis machine latest mode having bicarbonate cartridge
dialysis facility as a standard. Capable of performing double / single
needle dialysis with acetate and bicarbonate.
(2) Battery backup 30 minutes or more.
(3) Should have variable dialysis flow 300 to 700 in steps.
(4) Pressure monitoring at arterial and venous lines, blood pump with
flow rate 0 to 500 ml / min.
(5) Heparin pump administration flow rate monitoring.
(6) Temperature regulation and monitoring and adjustable
temperature.
(7) Conductivity regulation and monitoring. Conductivity based and
flow controlled concentrate dosing.
(8) Air detection ultrasonic.
(9) Disinfection procedure with heat/citric acid liquid citric acid or clean
cart.
(10) Assisted priming.
(11) Automatic self-test.
(12) Standby mode.
(13) UF profiling, step and interval, programmed or manual.
(14) Fully drainable single pass fluid path.
(15) Servo stabilizer with each machine.
(16) Detail regarding installation, post installation service both during
warranty period and after expiry of warranty.
(17) Automatic blood pressure monitor.
 b. Reverse Osmosis System with Each Machine. Water reverse
osmosis unit, multimedia/sand filter, water softener, activated carbon filter,
activated chlorine filter water pressure system complete, storage tank 200
gallons, Ultra Violet water sterilizer, product water 3-6 liter /minute.
3. Power Requirement
a. Line voltage: (220 V, +10%), 50 Hz
b. System should have built-in protection circuit against input high/low voltage
and short circuit.
4. UPS. It should have following features:-
a. Back up time 180 minute or more at full load
b. Switching time < 4 msec
c. Out put voltage 220VAC + 5% when input varies from 160 to 260 V
d. Wave shape Pure sine wave
5. Certificate. Certificate of having approval from Federal Drug Association (FDA)
USA or meeting the Japanese Industrial Standard (JIS) or European Standard Medical
Devices (ESMD) be provided.
 Portable Ultra Sonography With B & M Mode Imaging

1. General Ultra sound is an imaging investigation electro medical equipment. It

will use when the patient could not mobilized to main radiology department, or when
they are serious and require immediate report in emergency ward with latest software
for all applications and capable to be upgraded for 3 x dimension (3D)& 4 x dimension
(4D).
2. Physical/ Technical Characteristics
c. Scanning methods
(1) Electronic convex sector
(2) Electronic linear sector
d. Image Display Modes
(1) B-mode / dual mode
(2) M-mode
(3) BM-mode
e. Monitor Size 9 black and white monitor or better
f. Image gray scale 256 levels or better
g. Measurement / Analysis It should have comprehensive
measurement package for the measurement of distance, area, volume,
depth including abdomen general, gynae / observation, cardiac
calculations, urology and various reporting packages.
h. Console These ultra sound machines are portable; however, with trolley
they will be preferred. The machine should have a single active port with
option of two ports.
i. Probes. 3.5 MHz high resolution, high density, electronic, convex probe
(multi frequency probe capable to handles all types of frequencies of
ultrasound.
j. Storage Device. Cine memory > 32 images.
3. Accessories
a. Black & white printer (high quality)
b. Foot switch
 c. Biopsy adaptor (for convex probe)
4. Operating Conditions. System should be operable at 220 VAC + 10% at 50Hz.
5. Environmental Conditions
a. Operating temperature 10 ~ 40oC
b. Relative humidity 20% to 85%
6. UPS. It should have following features:-
k. Back up time 30 minute or more at full load
b. Switching time < 4msec
c. Out put voltage 220VAC + 5% when input varies from 160 to 260 V
d. Wave shape Pure sine wave
7. Certificate. Certificate of having approval from Federal Drug Association (FDA)
USA or meeting of Japanese industrial standard (JIS) or European Standard for Medical
Devices (ESMD) to be provided.
 INCUBATOR OXYGENIER
1. General. The equipment is required for the management of newborns / infants in
NICU.
2. Physical / Technical Characteristics
a. Servo control of incubator temperature by air & skin
b. Control mode Servo control range
c. Skin temperature setting
(1) Minimum 35oC or better
(2) Maximum 37oC or better
d. Skin temperature indication
(1) Minimum 36oC or better
(2) Maximum 38oC or better
e. Incubator temperature air
(1) Minimum 34oC or better
(2) Maximum 37oC or better
f. Incubator air temperature indicator
(1) Minimum 30oC or better
(2) Maximum 39oC or better
g. Accuracy + 0.5 oC
h. Humidity supply Adjustable from 40 to 90 % servo control
i. Oxygen supply Adjustable with external supply at least with
high and low pressure source 25%.
j. Noise level < 50 dB A
k. Alarms
(1) Temperature
(a) Air set temperature +1.5 C
(b) Skin set temperature + 1C
(2) System
(a) Power failure
(b) Air circulation failure
(c) Humidity sensor failure
 (d) Oxygen circulation failure
(e) Excess temperature
l. Display. Liquid Crystal Display (LCD)/ Thin Film Transistor (TFT) minimum
8.5 inches panel with trend display for air and skin temperature and
humidity. It should also display weight of baby.
m. Double wall hood on upper side.
n. 6 entry portsor better.
o. Air temperature probe.
p. Weighting scale incorporated to the bed.
q. X Ray facility while baby in incubator.
r. Intravenous (IV) pole facility should be present.
s. At least 2 x storage compartments.
t. Should have capability of SPO2(Oxygen saturation in blood) monitoring
preferably built-in.
u. Accessories
(1) Skin Temperature Probe 01
(2) Access Port Cover No 1 03
(3) Access Port Cover No 2 02
(4) Electrostatic Filter 01
(5) Air Leak Stopper 02
(6) Cap (rubber stopper) & Dust cover 01
3. Power Requirement
a. Power supply 220V + 20V AC, 50 Hz
b. The equipment should have built in self protection against surge/ high
voltage
4. Environmental Conditions
e. Operating temperature 10 to 35C
f. Storage temperature 0 to 60C
g. Relative humidity 5 to 99% non condensed
5. Certificate. Certificate of having approval from Federal Drug Association (FDA)
USA or meeting of Japanese industrial standard (JIS) or European Standard for Medical
Devices (ESMD) to be provided.
 Bedside Cardiac Monitor With Paediatric Probe

1. General. The equipment is used to perform the heart rate (HR), Electro Cardio
Graphy (ECG), Pulse Rate, SPO2, Respiration Rate (RR), Dual Temperature, CP2, Non
Invasive Blood Pressure (NIBP), Invasive Blood Pressure(IBP),End Tidal Carbon
Dioxide (EtCO2), body temperature, Cerebral state monitoring and alarm limit of patient.
2. Physical / Characteristics. System should have following features:-
a. Display TFT 12 inch or more.
b. Operation methods: Operation methods should be based on rotary
knob or membrane.
c. Sweep Speed Should be 12.5, 25, 50 mm/sec or more.
d. Wave forms: Wave forms should include Electro Cardio Graphy
(ECG), Oxygen concentration in blood (SPO2),
PLETH, Respiration, Electro Encephalography (EEG)
all should be freezable.
3. Technical Characteristics. System should have following features:-
a. ECG
(1) Leads Should have standard 3 leads extendable to 5 leads or
more.
(2) QRS detection duration
(a) Minimum 40 m sec or better.
(b) Maximum 120 m sec or better.
(3) Heart Rate Range Should have Heart Rate Range:-
(a) For adults 15 to 300 bpm.
(b) For Neonates 15 to 350 bpm.
(4) Protection Should be protected against deliberation and
electro surgery.
(5) Response time should be within 10 sec after cardiac arrest.
b. Arrhythmia Analysis
(1) Storage Real time arrhythmia detection
c. Stress Test (ST) Analysis Feature should include user adjustable,
Isoelectric and ST point trading of ST
values for an update period of 5 sec.
d. SPO2
(1) Pulse Rate Range Should have 25-250 bpm.
(2) MASIMO SPO2 should be MASIMO.
(3) % saturation range
(a) Minimum 40 % or better.
(b) Maximum 100 %.
e. Non Invasive Blood Pressure (NIBP)
(1) Measurement Measurement methods should be Oscillomatric
with manual and automatic measurement
modes (intervals between 5min-24 hours).
(2) Measurement Should have following ranges:-
Ranges For adults Systolic: 25-250mmHg, DIA:10-220
mmHg & MAP:15-250 mmHg.
For Neonates SYS: 25-135mmHg,
Diasystolic:10-110mmHg & Mean Arterial
Pressure (MAP) :15-125 mmHg
(3) Pressure transducer accuracy Should be + 3 at full range.
(4) Initial Inflation Target Should have :-
For adults: 150 breath per minute (bpm)
For Neonates: 70 breath per minute (bpm)
(5) Memory Should have minimum 100 records.
f. IBP
(1) Channels Should have 1 or more channels.
(2) Measurement Ranges Should have Range:-
Systolic: 50-300 mmHg,
Diasystolic:50- 300 mmHg
Mean Arterial Pressure (MAP): 50-300
mmHg
 g. Carbon Dioxide (CO2) Main Stream. Should have main stream
capnography along with side stream capnography preferably.
h. Respiration. Breath rate range 6 to 150 breath per minute (bpm).
i. Temperature. Body temperature measurement from 20 to 45OC or better.
j. Alarms. Alarms should include error message and the alert should be
blinking on display and volume adjustable with light indicator.
k. Trends
(1) Time Trend Time should be 1,2,4,8,16 and 24 hours or better
(2) Sources Heart rate (HR), premature ventricular contraction
(PVC), stress test (ST),SPO2,Respiration rate
(RR),Invasive Blood Pressure (IBP)1 (Systolic,
diasystolic, mean arterial pressure (MAP)Invasive
Blood Pressure(IBP)2 (Systolic, diasystolic, mean
arterial pressure (MAP), Temperature1, temperature
T2, end tidal carbon dioxide ( EtCO2), fractional
concentraion of O2 FiO2,EtAA, FiAA
l. Input / Output
(1) Capability of connecting with the networking system at central monitor
4. Power Requirement
a. System should be operable on 220V + 10%, 50Hz.
b. The internal battery should be rechargeable with more than 1 hour
continuous use.
5. Environmental Parameters
a. Operating temperature 10C ~ 40C
b. Relative humidity 20% ~ 85%
c. Accessories
(1) Temperature probe.
(2) SpO2 probe: one for adult and one for infant.
(3) Electro Cardio Graphy (ECG) cable three lead.
(4) Non invasive Blood Pressure (NIBP) cuff with tube: one for adult
and one for infant.
 (5) End tidal carbon dioxide (EtCO2) probe/ module.
(6) Operating manual.
(7) Technical manual.
(8) Trolley to mount apparatus
6. Stabilizer. Servo type voltage stabilizer be provided along with the equipment.
7. Certificate. Certificate of having approval from Federal Drug Association (FDA)
USA or meeting of Japanese Industrial Standard (JIS) or European Standard for
Medical Devices (ESMD) be provided.
 16 Slice Computer Tomography (CT)

1. General. 16-Slice computer tomography (CT) system provides exceptional

image quality with single console interface. It features fast and efficient image
reconstruction, giving clinicians access to high quality images and powerful diagnostic
tools, enhancing workflow productivity and clinical outcome.
2. General Characteristics. The system should have following characteristics:-
h. Easy to operate / user friendly.
i. Fully automatic operation.
j. Multi slice, high speed detectors of variable thickness to acquire accurate
isotropic data per rotation.
k. High resolution / quality, finely detailed 3D images generation.
l. High quality 3D images generation with bone segmentation.
m. High quality 3D image generation with bone removal feature to ensure
highly accurate & diagnostic computer tomography (CT) angiograms.
n. Automatic filter to adjust tube current to reduce the exposure dose
preferably computer controlled.
o. Dose optimized for each patients anatomy.
p. Multi slice computer tomography (CT) fluoroscopy for real time image
reconstruction to display at least 3 images obtained by combining data.
q. High quality 3D images for complete and accurate assessment of blood
supply to the brain.
r. Three dimensional display of surfaces with different density values soft
tissue bone contrast enhanced vessels.
s. Picture Archiving and communication system (PAC) compatible, compliant
machine / system.
3. Physical & Tech Characteristics
t. Gantry. Should have following features / specifications:-
(1) Spiral / helical acquisition modes.
(2) Continuously rotating tube detector unit for high resolution data
acquisition across the entire scan field.
 (3) Aperture 70cm atleast.
(4) Scan field 50 cm atleast.
(5) Tilt + 30. Preferably remote control assisted from console.
(6) Rotation Time (variable) 0.6 - 0.8second / 360o or less.
u. Data Acquisition System. Should have following features:-
(1) Scan region Whole body including head.
(2) Scan system 360, continuous rotation.
(3) Scan planning programmable.
(4) Maximum no of slices / rotation - 16
(5) No of physical detector rows - 16 or better
(6) Symmetrical Isotropic Resolution < 0.6 x 0.6 x 0.6
(7) Slice thickness variable (Min) 0.5mm or better
(Max) 20 mm or better
(8) Detector type - Ultra fast ceramic / solid state detectors or better
(9) Image reconstruction time 10 images / sec or better
(10) Real time image display matrix 1024 x 1024 or better
v. X-Ray Tube Assembly. Should have following features:-
(1) Exposure Continuous
(2) Tube current (Minimum) 10 m A,
(Maximum) > 300 m A
(3) Tube voltage (variable) (Minimum) 80 KV,
(Maximum) 130 KV or better
(4) Anode Heat Storage Capacity 4-8 Mega Heat Unit (MHU) or
better
(5) Focal spot size < 1.0 x 1.0 mm (small)
<1.4x 1.4 mm (large)
(6) Computer controlled monitoring of anode temperature.
(7) X-Ray generator > 80-135 KW high frequency
air cooled
(8) X-Ray tube filter installed in collimator, preferably computer
controlled for dose reduction.
 (9) X-Ray tube filter 6.5 mm Al equivalent or better.
(10) Collimators filter 0.5 mm Al equivalent or better.
(11) Automated real time tube current adjustment for best quality image
at lowest possible dose, independent of patient size and anatomy.
(12) Special X-Ray exposure protocols / settings for minors / children.
(13) Anode heat dissipation 700Kilo Heat Unit (KHU) or better
w. Acquisition Console. Should provide an intelligent and reliable work flow
for data acquisition, image reconstruction and routine post processing.
Should be a branded system with following minimum specifications:-
(1) Processor Dual core Pentium 2.66 Giga Hertz (GHz) or better
(2) Suitable graphics card for fast 3D post processing.
(3) Monitor 17Liquid Crystal Display (LCD) / Thin Film Transistor
(TFT) / Light Emitting Diode (LED) flat screen.
(4) Resolution > 2 Mega pixel
(5) RAM 4 Giga Byte (GB) or better.
(6) Hard disk 500Giga Byte (GB) or better.
x. Additional Storage
(1) Compact Disc Reader / Digital Video Disc, Read Only Memmory
(ROM) / magneto optical disc.
(2) External USB2.0 interface optional.
y. Computer Tomography (CT) Work Station. Computer Tomography
(CT) work station is a separate / dedicated computer tomography (CT)
processing work station. Should be a branded system with following min
specification:-
(1) Processor 2 x dual core or better
(2) Random Access Memmory 4 Giga Byte (GB) or better
(3) Suitable graphics cards for fast 3D post processing.
(4) Monitor 17 flat screen Liquid Crystal Display (LCD)/ Thin Film
Transistor (TFT) / Light Emitting Diode (LED)
(5) Resolution > 2 Mega pixel or better
(6) Image storage Shared database with acquisition workplace
 (7) Write / Reader- Compact Disc (WR/CD) / Digital Video Disc
(8) Local Area Networking (optional) 1 Giga Byte (GB) Card
z. Digital Imaging and Communication System (DICOM 3.0) System should
be DICOM 3.0 compatible, compliant. Full features must be available
including following:-
(1) Digital Imaging and Communication System (DICOM) print
(Essential).
(2) Digital Imaging and Communication System (DICOM) storage
(Optional).
(3) Digital Imaging and Communication System (DICOM) get work list
(Optional).
(4) Digital Imaging and Communication System (DICOM) send.
(5) Digital Imaging and Communication System (DICOM) receive.
(6) Digital Imaging and Communication System (DICOM) archive.
(7) Digital Imaging and Communication System (DICOM) retrieve.
aa. Software. Software should be included as per user requirement. Should
have following features:-
(1) Picture Archiving and Communication System (PAC) compatible,
compliant system.
(2) Real time topogram.
(3) Patient breath hold time indicator.
(4) Automatic patient positioning.
(5) Multi slice spiral acquisition.
(6) Gantry tilts control from console.
(7) Reconstruction modes:-
(a) Full image.
(b) Half image.
(c) Detail image.
(8) Region of Interest (ROI) parallel evaluation of 3 ROI or better.
(9) Automatic display of reconstructed images.
(10) Filter parameter customization through on screen menu selection.
 (11) Images rotation feature.
(12) 3D display of surfaces with different density values.
(d) Soft tissues.
(e) Bone.
(f) Contrast enhanced vessels.
(13) Image zoom and pan.
(14) Full color volume rendering 3D at console / workstation.
(15) Isotropic volume acquisition at console.
(16) 3D surface rendering at both consoles and workstation.
(17) Curved planer reforming at console.
(18) Virtual endoscopy / colonoscopy / bronchoscopy at workstation /
console.
(19) Head perfusion both at console and workstation.
(20) Lung nodule
bb. Multi Slice CT Fluoroscopy. Should have Intervention computer
tomography (CT) Fluoroscopy capability.
(1) Multi Slice fluoroscopy with real time imaging and display with at
least 12frames / sec with required hardware / software.1 x high
resolution 17inch or more Light Emitting Diode (LED) / Liquid
Crystal Display (LCD) / Thin Film Transistor (TFT) monitor in the
computer tomography (CT) room.
(2) Digital Imaging and Communication System (DICOM) compatible
digital / dry laser / thermal camera up to 14 x 17 for automatic
digital filming.
(3) Biopsy mode with user configurable dose selection.
(4) Real time dose modulation during computer tomography (CT)
guided intervention.
cc. Treatment Table. Should have following features:-
(1) Table load capacity 200 kg or better.
(2) Fully motorized table motion.
 (3) Alignment lights in gantry aperture for fast and accurate patient
positioning.
(4) Safety features to include following:-
(g) Electromagnetic brakes.
(h) Automatic brake activation in the event of power failure.
(i) Motion stop buttons on both sides of console preferably.
(j) Ability to lower table in the event of power failure.
(k) Tabletop lock indicated visually.
(5) Carbon fiber tabletops.
dd. Power Supply
(1) 3 phase 4 wire sys 400 V+ 10% 50 Hertz (Hz)
(2) System should be protected against input power instability.
(3) System should have electromagnetic compatibility with
IEC60601-2.
(4) Suitable Uninterrupted Power supply (UPS) with at least 10 minutes
backup time on full load.
(5) Automatic voltage regulator
ee. Examination Room Environmental Conditions
(1) Op temp range 10C to 40C
(2) Relative humidity 20 85% no condensation.
ff. Accessories
(1) Digital Imaging and Communication System (DICOM) compatible
dry laser images for film size 14 x 17
(2) On line sine wave Uninterrupted Power supply (UPS) for whole
computer tomography (CT) suite, with a minimum backup of 10
minutes on full load
(3) Dual head programmable, power injector with flow / volume and
temperature control for both head independently, mounted on
mobile base / ceiling suspended with 100 syringes of 150ml
capacity and connecting tubes
 (4) Standard set of phantoms for calibration of computer tomography
(CT)
(5) Table accessories
(l) Table pad
(m) Arm rest
(n) Patient restraint kit
(o) Intravenous (IV) pole
(p) Infant cardiac
(q) Flat head holder
4. Certificate. Certificate of having approval from Federal Drug Association (FDA)
USA or meeting the Japanese Industrial Standards (JIS) or European Standards for
Medical devices (ESMD) be provided.
 Bronchoscope

1. General. It is essential equipment required for examination suffering from

disease of trachea and bronchi.
2. System for Bronchoscopy
a. Flexible Endoscope with Suction Valve for use with Monitor
(4) Deflection up / down -130o to 180o or better
(5) Direction of view 0o
(6) Angle of view 120o - 140o or better
(7) Working length 55 70cm
(8) Working channel inner diameter 2.3mm or more
(9) Distal tip outer diameter 5 mm or more
b. Consisting of
(1) Flexible endoscope case
(2) Pressure compensation capability
(3) Leckage tester
(4) Tube holder
(5) Cleaning brush
(6) Irrigation adopter
(7) Suction valve
(8) Bronchoscope insertion tube, size 4-6mm
(9) Plug, package of at least 10
(10) Protection capability for use
c. Monitor for Endoscope, size 17, Video Graphic Array (VGA)
Resolution or better
(1) Video output Composite NTSC signal or other enhanced
image quality, splash proof, suitable for wipe
disinfection, shock resistant plastic housing
and intelligent power management with
rechargeable Li-ion batteries or better video
and image documentation in real time should
 be stored directly on USB or SD card or other
devices or better sys.
(2) Camera, Full High Definition (HD) Camera with CCU. Should
have camera system with following features:-
(a) Full High Definition (HD) camera system with camera head
complete.
(b) Full High Definition (HD) 3 chip camera system with 1080p
60 f / sec or better
(c) Charge Couple Device (CCD) (inch) 3 x 1/3 or better.
(d) Camera resolution >2Mega pixel or better.
(e) Scan mode progressive scan 60 hertz or better.
(f) Modes 5 presetting, 3 user setting or more.
(g) Video signal outputs.
(h) DVI-D 1080 (50/60 Hz) HD SDI 1080i, 720p (50/60 Hz) or
better.
(i) HD RGB 1080i, 720p (50/60 Hz), S-Video NTSC, video
composite NTSC or better.
(j) 2 button on camera head with 6 functions or better.
(k) Digital zoom (2x)
3. Power Supply 220VAC + 10%, 50 Hz
4. Consisting of Protection capability
5. At least 2 biopsy forceps, flexible, spoon shaped, round, double action jaws,
diameter 1.8mm.
6. At least 2 grasping forceps, flexible, alligator jaws, double action jaws, diameter
1.8mm work.
7. Stainless steel made stand for mounting or other.
8. Certificate. Certificate of having approval from Federal Drug Association (FDA)
USA or meeting of Japanese Industrial Standard (JIS) or European Standard for
Medical Devices (ESMD) be provided.
 Real Time Polymerase Chain Reaction (PCR) Thermal Cycler
(Open System)

1. General. This machine is required for real time amplification of bacterial, viral and
cellular genes. It is suitable both for research and diagnostics.
2. Physical and Technical Characteristics
a. Thermal Performance
(1) Thermal block format 96 wells or better
(2) Temperature accuracy 0.2 0.5 + 0.02 (standard deviation)
(3) Average ramp rate (Average 3 3.7oC)
(4) Heating and cooling method 3.3oC / sec
(5) Lid temperature
(a) Range 0 105oC
(b) Accuracy +0.2oC of programmed target at 90oC
(c) Uniformity +0.4oC well to well within 10 second of
arrival at 90oC
(6) Gradient
(a) Operational range 30 100oC
(b) Programmable span 1 24o
(7) Optical System
(8) Excitation 5 6 filtered Light Emitting Diode (LED) or better
(9) Detection 5 6 filtered photodiodes or better
(10) Dynamic range 10 orders of magnitude
(11) Range of excitation / emission 450 730 nanometer (nm)
wavelength
(12) Sensitivity Detects 1 10 copy of target sequence in human
genomic Deoxyribose Nucleic Acid (DNA)
(13) Scan time
(a) All channels 12 sec
(b) Single channel fast scan 3 sec
b. Thermal block format 96 test tubes or better
 c. Display Thin Film Transistor (TFT) / Liquid Crystal Display (LCD) / Light
Emitting Diode (LED)
d. Electrical Requirement
(1) Power Voltage 220 + 10%, 50 Hz
e. UPS Should be provided with following features:-
(1) Back up time 30 minutes or more at full load
(2) Switching time < 4ms
(3) Wave shape Pure sine wave
(4) Voltage stabilization Output 220VAC + 5% when input
varies from 160V to 260V
f. Multiplex analysis Upto 5 targets per well
3. Certificate. Certificate of having approval from Federal Drug Association (FDA)
USA or meeting of Japanese Industrial Standard (JIS) or European Standard for
Medical Devices (ESMD) be provided.
 MAGNETIC RESONANCE IMAGING (MRI) SYSTEM

1.
4. Introduction. Required for diagnosis of Brain, Spine and Joints. There are many
diseases which can be diagnosed on MRI only.
5. Physical/Technical Characteristics
a. Magnet Subsystem
(1) Magnet length 160cm or less.
(2) Field Strength 1.5 Tesla.
(3) Shielding Active
(4) Shimming Passive/Dynamic/Active.
(5) Field In homogeneity 0.1 PPM/ hour or less.
(6) Tunnel diameter 60cm or more.
(7) Cryogen Helium.
(8) Cryogen boil off rate 0.05 L/hour or less.
(9) Cryogen Refill interval 03 years or more.
(10) Safety Features Emergency shut down and
cryogen leak alarm.
b. Gradient Subsystem
(1) Type Actively shielded (water cooled).
(2) Gradient Field Strength 40 milli tesla per meter or more.
(3) Slew rate 150 T/m/s or more.
(4) Slice thickness 0.5 mm or less for 2 DFT and
0.05 mm or less for 3DFT images.
c. RF Subsystem
(1) Type Digital.
(2) Transmitter Power 20 KW or more fully digital.
(3) Spectrometer type Direct digital sampling.
(4) Should have minimum of 8 receiving independent RF channels.
(5) Should have necessary hardware to software phased array coils.
 (6) Should be compatible with parallel imaging technique and should
support time reductions with compatible coils in 2D / 3D imaging for
body / neuro by factor of 4 (at least).
(7) Should include RF cabin and RF shielding.
d. Computer
(1) Type Real time inter-active control
processor, with multitasking
capability, system should be
upgradeable and have real time
network connectivity.
(2) Clock speed 2.8 GHz or more.
(3) RAM 3 GB or more.
(4) Storage devices Hard disc of 500 GB or more and
matching high capacity DVD with
erasable components.
(5) Image reconstruction 5500 images/second or more.
(6) Application software DICOM 3.0.
e. Main Console
(1) Monitor 21 LED inches or better, colored,
high resolution (matrix 1024 x 1024 or
better) with 256 or better
Grayscale, flicker free.
(2) Other devices. CD-ROM, Keyboard, Mouse.
f. Additional Independent Work Station
(1) With full image post processing capability and surface shading.
(2) The monitor should be 21 LED or more in size, should be colored
with high resolution 2048 x 2048 matrix or better and have real time
network connectivity.
(3) Should be flicker-free, capable of inter-active windowing with
geometric manipulation, stock and file viewing.
(4) Should be fully compatible with the MRI scanner.
 (5) Should have a laser printer (A-4 size with 2400 DPI).
(6) The station should be able to work independently, even when MR
system is not working.
(7) The system should have DICOM 3 connectivity.
g. Films Printing. Latest Dry LASER day-light camera and automatic
Printing system for 14x17 films from a reputable manufacturer
(Kodak/Agfa/Fuji).
h. Patient Table
(1) Fully motorized.
(2) Weight bearing capacity: 200 Kg or more.
i. Patients Comforts
(1) Light, intercom and music system.
(2) Patient Monitoring Vital signs, CCTV etc.
(3) Standard Paediatric accessories.
(4) Gating facilities for Pulse, ECG and Respiration.
j. Coil Sets
(1) Coils must comply with matrix or array coil technology and must be
compatible with PAT (Parallel Acquisition Technique):-
(a) Whole body array coil Quadrature / Cerebral Palsy (CP)
(b) Spine coil (to cover whole spine)
(c) Head coil
(d) Knee Coil
(e) Neck coil
(f) Body coil (for thorax, abdomen and pelvis). Capable of
Magnetic Resonance Chalangiopancreatography (MRCP)
and peripheral imaging. At least 16 elements and 15cm
FOV.
(g) Shoulder coil
(h) Set of multi-purpose flexible coils
(i) Breast coils
(j) TMJ coils (Bilateral)
 (2) All coil sets should be complete in all respects so that they are
operationally functional and patient ready.
k. Imaging Packages
(1) The system should be complete with all standard packages
including the following:-
(a) Conventional Scans Routine (density imaging) T-1, T-
2 Proton density, FS and FLAIR
imaging
(b) Fast/Turbo scans SE, FFE, IR, Turbo/ Fast SE
(c) EPI (single & multi shot)
(d) Advanced Scan 3D, STIR, real time, cine mode,
MRCP, MR Urography, MR
Myelography, MR Cardiography
Quantitative flow (for CSF)/ blood
flow direction)
(e) MR Angiography (peripheral/body) with 2D/3D TOF and
phase contrast sequences.
(f) Ultra-fast SE imaging with more than 200 ETL
(g) Fat / Artefact / Motion suppression techniques.
(h) Diffusion, Perfusion and Functional MR imaging capabilities
(with generation of ADC maps).
(i) Parallel Acquisition Technique (PAT)
(j) The system should have spectroscopy package (hydrogen,
single and multi voxel).
(k) Diffusion Tensor Imaging (DTI) package.
(l) Whole body scanning/screening with stitching facility.
(m) UPS capable to operate the whole system with at least 30
minutes back up.
6. Environmental Conditions
a. Operating temperature 15-28C
b. Relative humidity 15% - 75%
7. Reliability and Maintenance
a. Reliable in terms of performance
b. Easily installed
c. Low maintenance cost
d. Spare parts readily available
e. Availability of qualified Engineers with supplier for maintenance
8. General Notes
a. The system should be the latest 1.5 Tesla system including latest software
and hardware.
b. The firm will ensure software upgrades free of charge.
c. System should be complete with non-magnetic patient trolley, metal
detector, MR compatible patient trolley and wheel chair with an IV pole,
MR compatible automatic I.V contrast injector and MR compatible general
anesthesia machine for children and uncooperative patients.
d. Standby compatible diesel generator of a well known international make
for the entire system would be supplied and maintained as part of the
contract. The generator must have an auto changeover facility. The cable
from generator to the system would be supplied by the firm.
e. An extra chiller for the whole system would be provided.
 FOLDING WHEEL STRETCHER

4. Details of Equipment
a. General. Shifting of patients from hospital ward to OT, other clinics
and laboratories for various medical procedures usually required two
nursing staff which at time results in delays due to non availability of the
second attendant. Therefore a wheel stretcher capability of being handled
by a single attendant is required. It should facilitate boarding/de-boarding
of patient from ambulance without trouble/jerk with excellent mobility and
easy of maintenance.

b. Frame. It must be robust enough to sustain the average weight of

patient laid on it. It should be strengthened by supporting rods.

c. Locking Mechanism. It should be firmly locked on the floor of

ambulance.

d. Boarding/De-boarding of Patient. Boarding/de-boarding of patient

especially surgical patient into / from the ambulance on stretcher must be
trouble/ jerk free.

e. Stability. It should be quite stable during move.

f. Lever / Locking Mechanism of Wheels. It should have locking

mechanism on head-side of wheels during de-boarding.

g. Mobility on Surface. While moving on even surface patient should

not feel jerk / discomfort. It must be trouble free on uneven surface.

h. Feasibility. It should be quite feasible to meet the hospital and peace

requirement.
i. Type of Wheels. Suitable for use on any surface i.e. gravel, cemented,
road, ground etc.
j. Mattress. Suitable to fit in the main frame.
k. Weight. Not to exceed 45 kg.
l. Technical Requirements

(1) Dimensions of Main Frame

(a) Unfolded / Open

i. Length - 1905 mm.
ii. Width - 548 mm.
iii. Height - 818 mm.
(b) After Folding
i. Length - 1905 mm.
ii. Width - 548 mm.
iii. Height - 275 mm.
(2) Side Support for Patients
(a) Height
i. Maximum - 185 mm.
ii. Minimum - 175 mm.
(b) Length - 800 mm.
(3) Length of Stretcher Legs. Front/ Rear (Max) 610 mm
m. Additional Requirement. Should have suitable arrangement for
hanging glucose bottles, blood bags etc, during transportation of patients.
 AUTOCLAVE 1000 L

4. General. The eqpt is used for sterilization of instruments under medical usage. It
is used to control cross infection and kill bacteria, viruses (HBV, HCV & HIV) including
resistive spores.
5. General Requirements / Features. System should have following features:-
a. Large Steam Sterilizer with built in 72KW or better Steam Generator.
b. Provision of connection for external steam supply.
c. Chamber capacity Minimum 1000 liter.
d. Chamber constructed of high grade stainless steel.
e. Auto drainage system.
f. Fully automatic, microprocessor type and programmable for textile solid,
hollow, rubber and plastic stores in terms of time, temperature, pressure
and no of cycle.
g. Auto air leakage detection system.
h. Sterilizing temperature range 105C to 135C.
i. Automatic single counterbalanced horizontal sliding / vertical door.
j. Should have pass through double door system.
k. Sterilizing cycle capacity 20 cycle including medical cycles, waste cycles
and laboratory cycles.
l. High performance vacuum system and a silicone sealing gasket.
m. Safety interlock system.
n. Emergency OFF switch.
o. Pressure release valve.
p. Automatic water level control.
q. Automatic boiler blow down system.
r. Low water level protection system for heating element.
s. Pressure booster pump for low water supply pressure.
t. Recording system.
u. Cycle indicator to determine the phase of sterilization cycle.
 v. Alpha numeric visualization of sterilization parameter on touch screen with
display of the remaining time.
w. Complete standard accessories, all alarms and removable shelves.
x. External mobile trolleys with swivel castor and internal loading carriage.
y. Built in thermal printer.
z. Built in standard protocol for sterilization of items having material of
different types, i.e., steal, cloth, rubber etc.

6. Power Supply. Should operatable at 440VAC + 10%, 50/60 Hz 3 phase

7. Environmental Conditions

a. Operating temperature 0-35C

b. Humidity 30-75% RH

8. Standards. Certificate of having approval from Federal Drug Association

(FDA,USA) or meeting the Japanese Industrial Standard (JIS) or European Standard
Medical Devices (ESMD) be provided.