anaesthesia department · anaesthesia department. specification of anaesthesia work station -o. 2,...
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ANAESTHESIA DEPARTMENT
SPECIFICATION OF ANAESTHESIA WORK STATION
- O2, N2O & Air flow meter
- Should have facility to give low flow anesthesia
- Should have safety features for Oxygen failure alarm, minimum Oxygen flow & hypoxic
guard.
- Should have integrated ventilator with at least pressure support, PEEP, FiO2 with battery
backup
- Should have integrated multimonitor with battery backup with following parameters:
(a) Pulse oximetry-with one adult & one pediatric probe
(b) Capnography- Side stream type with inspired & Et CO2 ,inhalational anesthesia
agent monitoring with MAC values & graphic representation of Et CO2
(c) ECG Monitoring- 5 leads ECG
(d) Temp. monitoring- with one skin & one rectal probe
(e) NIBP- with one adult, one pediatric & one neonatal cuff
(f) Provision for invasive BP monitoring
- Should have closed circuit with circle absorber
- Proper space for keeping drugs & disposables
- Adequate drawers to keep accessories
- Silicon reusable circuits- one adult & one pediatric
- Machine should be supplied with suitable UPS
- Should have FDA/CE approval
Accessories:
1. Moisture trap for EtCO2 module=20
2.Capnograph lines=30
SPECIFICATIONS OF CARDIAC MONITOR DEFIBRILLATOR AND RECORDER
Should be Biphasic Defibrillator, monitor with recorder .
Should have facility for automatic external defibrillator (AED) and Manual Defibrillator.
Should have facility for 3/5 lead ECG Monitoring and Synchronized Cardio version.
Should have Adult and Pediatric Paddles.
Should have ten second charging time for maximum energy.
Built in charger.
Charging should be through paddles also.
Should work on 210-230 volts.
Battery back up for discharges.
Multiple viewing angles for clear visibility.
Should have built in Strip Printer.
Should have facility for printing critical events.
Facility for in built SpO2 monitoring .
User selectable low and high Heart Rate alarm.
Low SpO2 alarm.
Facility for in built Pace-Maker (non-Invasive)- demand and non-demand type pacing.
I.E.C.or equivalent safety certification.
FDA / CE or equivalent certification.
Essential Accessories
1. Trolley: Good quality rust proof material with castors and break, with one drawer to keep
accessories.
2. SpO2 Probe Adult and Pediatric.
3. Pacing Pads.( one box of 10 nos.)
SPECIFICATION OF MULTIPLE VITAL SIGN MONITOR (MULTIMONITOR)
1. It should have modular design with colour coded interchangeable modules.
2. It should have valid FDA approval and CE certification
3. It should function on AC mains and should have rechargeable internal battery of more
than 2 hrs capacity.
4. Monitor should have port for connectivity to central nursing station and hospital local
networking system.
5. It should have bright and highly visible TFT screen display of 14” to 18”.
6. Should have capability to monitor at least 6 real time wave forms along with related
numerical parameters on a single configurable screen.
7. It should monitor SPO2, pulse rate, ECG, NIBP, Respiration, 2 temperatures, 2 invasive
pressures, Respiratory gas monitoring for E+CO2 with provision of suitable audio visual
alarms.
8. It should have capability to monitor the above parameters in adult, pediatric and patients.
9. The size of numeric and wave forms should be adjustable.
10. Colors of display of various parameters should be interchangeable.
11. It should have facility for monitoring 12 lead ECG including 12 lead ST segments
through 5 lead ECG cable.
12. It should have a minimum of 24 hours graphical, tabular trending facility.
13. It should have advanced multilead arrhythmia analysis capability.
14. Standard accessories and peripherals for monitoring the parameters mentioned in Para 7
audit, pediatric and patients should be provided.
BLOOD BANK
SPECIFICATION OF AUTOCLAVE
1) Electrically operated ( 220 V- 240 V)
2) Vertical type
3) Should be double walled
A) Inner wall made up of S.S.
B) Outer wall made up of M.S. / S.S.
4 ) Size 550mm x 350 mm ( approx )
5 ) Lid should be made up of stainless steel & provided with tightening device
6)Should have pressure gauge, water level indicator , steam release valve &
safety valve & drain for emptying the Autoclave .
7)Joint less Gasket in one piece
8)Working pressure 10psi to 20psi .
9)To be supplied with cord, plug & stainless steel basket .
10)Should have a pedal lifting arrangement to lift the lid.
SPECIFICATION FOR BLOOD BANK REFRIGERATOR
1. Capacity of 500-600 Liters or more.
2. Capacity to hold Minimum of 300 blood bags of 450ml.
3. External Construction-- MS
Internal Construction –SS
4. Should have 4-6 fully extendable, solid bottom, stainless steel drawers with smooth
sliding and locking system and drawer dividers.
5. Lockable castors
6. Should have adjustment for uneven bases.
7. CFC free insulation
8. temperature range+2 to +4o C + 1o C.
9. Positive forced air circulation to maintain temperature uniformity in all the areas of the
cabinet
10. CFC free hermetically sealed compressor
11. Capable of operating at ambient temperature upto +43o C
12. Automatic defrost
13. Automatic condensate removal with no requirement for separate drainage lines
14. Heated dual pane insulated glass door with safety lock and key
15. Interior fluorescent light
16. Large and clear digital display for set/run parameters.
17. Weekly, circular, inkless, temperature Chart Recorder.
18. Independent microprocessor temperature controller
19. Independent alarm and monitor system with battery backup of apprx. 4 hours,
Audio-visual alarm for high and low temperature, power failure, door open and sensor
failure
20. Temperature recorder probe ,independent from other probes for connection to data
logger
21.220-240 volts/50Hz
22. Suitable voltage stabilizer compatible with the equipment to be provided.
23. Should be CE/FDA/BIS approved
24. Electrical safely certification
25. User/Technical/Maintenance manual to be provided in English
26. Logbook with instruction for daily, weekly, monthly, quarterly maintenance checklist, the
job description of hospital technician and company service engineer should be clearly spelt out.
BLOOD COLLECTION MONITOR
• Should have complete flow cut-off when collection weight is reached.
• Should have battery operation for mobile use
• Should be display collection start & finish time.
• Should be suitable for mobile environments.
• Should automatic tare to zero for the bag weight
• Should calibrates in less than 15 minutes
• Should have donation time upto 20 min
• Power Consumption should be max 10 VA
• Should have48 hs. Battery backup,
• Accuracy - <1% of max weight +/- 1 ml
• Measuring range should be up to 999 ml.
• Should have alarms for – Low Battery, under weight, over weight, Taring Error, set up
Error, Motor Error, Abnormal Blood flow, Time Over.
• Should have option for Barcode reader.
• Real time flow rate indicators assist phlebotomists without alarming donors...
• Weight should have approx. 5.5 kg.
• Should work at AC supply of 220-240V 50-60Hz.
• Should be FDA / CE or BIS approved product
SPECIFICATION FOR -30OC DEEP FREEZER
1. Should be of 4-6 drawers with 300 to 380 L capacity and a microprocessor temperature
controller with build in alarms monitor, front loading.
2. Should have adjustable temperature range of -10O to -40O C
3. Electrical refrigeration system defrost can be programmed to actual time desired,
allowing defrost cycle to run automatically during low use period.
4. Controller to be equipped with a temperature probe mounted in the system.
5. Digital calibration offset adjustment for controller calibration.
6. Four inch seven day circular chart recorder with following features:
a) Inkless ,pressure –sensitive chart paper with range of -50O C to 0O C
b) Electronic drive mechanism for consistent results.
c) Battery backup insures continuous operations.
d) Touch button controls for chart changes and calibration.
e) Power status indicator.
7. Refrigeration system:
a) Heavy duty, air cooled refrigerated system
b) Non-CFC, Commercially Available Refrigerant.
c) Internal evaporator is standard.
d) Internal evaporator fan(s) shut off during door opening.
e) Forced air circulation maintaining chamber uniformity of + - 1O C and provide
quick recovery.
f) Balance flow refrigeration system eliminate defrost cycle and maintains constant
temperature.
8. Cabinet :
a) Exterior, interior and door handler(s) made from galvanized steel with bacteria –
resistance powder coating.
b) Superior engineered frame for maximum rigidity.
c) Contoured door handling.
d) Non CFC foamed urethane insulation.
e) Heated, dual-pane, insulated glass door(s) remove fogging and condensation.
f) Standard key lock.
g) Drawers are stainless steel to guard against rust and corrosion.
h) Swivel locking caster
9. Drawers:
a) Solid stainless steel pulls out drawers.
b) Adjustable SS shelves
c) Easy access to inventory with fully extendable drawer slides.
10. Audio visual electronic alarm system independent of power supply
11. Suitable UPS for minimum of 30 minute backup
12. Overcurrent breaker
13. Operable continuously at ambient temp. of 100 to 450 C
14. FDA, CE or BIS approved product
TECHNICAL SPECIFICATION OF FULLY AUTOMATIC WALK AWAY
ELISA/IMMUNOASSAY
• ELISA System is required to Read the color change in ELISA Plates and Strip, automatic
programmable washing & dispensing system high throughput.
• Fully automated ELISA system with 4 microplates assays modular design for reader,
washer & incubators.
• Integrated robotic sample processor. Should have an open system for different makes kits
& manual over ride.
• Predilution facility should be presented.
• Random access, provision for multiple assays.
• Parallel sample pipetting should be present.
• 6 filters with a minimum range of 400-700 nm are required.
• Minimum 12 measurements.
• 16 ways manifold washing with minimum 4 wash channels.
• Volume of wash liquid dispensed variable & intervention.
• Residual volume/ well should be <2µl.
• User friendly software with option for manual intervention.
• Temp. range - room temp to 45 deg C +/- 1⁰ C.
• Plate incubator
• Liquid & clot/foam/bubbles detection should be present.
• Color monitoring check should be provided
• There should be no carryover of sample
• Password protection to prevent unauthorized person’s access to software.
• Printer to provide printed reports of testes. Patient name , ID keyboard entry & individual
report printouts in preset ID keyboard entry & individual report printouts in preset format
• Teflon coated metal probes.
• Facility to store at least 50 assay protocols.
• Facility to program samples, standards and controls in replicates
• Display of assay scheduling , start and finish times
• Automatic quality control equations like Westgard rules, Levy Jennings charts.
• Curve fits like Cubic Spline, Sigmoid, Polygon, Log, 4-parameter, point to point, Linear,
Quadratic, spline, lin/log
Reader Specification
• Dynamic range 0.0-3.0 OD
• Precision <2% CV(2-3.0 OD)
• Linearity +/- 1%(<2.00 OD)
• Accuracy +/- 0.005 OD or 2.5%
Washer Specification
• Manifold configuration 8 – 12way
• Wash cycle possible- Not less than 5
Incubator Specification
• Temperature minimum range - 25-400C
• Temperature Accuracy- +/- 10C
Facility for shaking
• Sample pipetting-
• Precision at 25µl <3% CV
• Accuracy at 25µl +/-2%
• Dispensing volume minimum 5µl
Reagent pipetting-
• Reagent pipetting precision <3% CV
• Reagent pipetting precision +/-2%
• System as specified.
• All consumables required for installation and standardization of system to be given free
of cost standardization of system to be given free of cost.
• The unit shall be capable of being stored continuously in ambient temperature of 0-50
deg C and relative humidity of 15-90%.
• The unit shall be capable of operating continuously in ambient temperature of 0-50 deg
C and relative humidity of 15-90%.
• Power input to be 220-240VAC,50Hz fitted with Indian plug.
• Resettable over current breaker shall be fitted for protection.
• UPS with 30 mints. Backup
• Comprehensive training for lab staff and support services till familiarity with the system.
• Five years warranty, 5 yrs comprehensive AMC should be available with service centres
in close proximity.
• Should be manufacturers to ISO 13485: Quality system- medical devices – particular
.requipments for the application of ISO 9001
• Applicable to manufacturers and service provides that perform their own design
activities.
• Should be FDA /BISor CE approved product.
• User/technical/maintenance manual to be supplied
• Certificate of calibration and inspection from factory.
• List of equipment available for providing calibration and routine maintenance support as
per manufacturer documentation in service/ technical manual.
• 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 spelt out.
• List of important spare parts, printer paper and accessories with their part no. and costing.
CARDIOLOGY DEPARTMENT
SPECIFICATION FOR ECG MACHINE 12 CHANNEL
Simultaneous acquisition of up to 12 leads.
Real time continuous recording of 3,6 & 12 channel.
Recording speeds of 5,10,25 or 50 mm/sec
Extension ECG quality control by AC noise filtering & baseline.
A4 size reports for convenient reading& filing.
Color coded keys for case of operation.
Convenient battery operation for greater mobility.
Versatile report formats & speed options to provide auto reports or rhythm report.
User configurable filters.
Preview signal quality prior to printing, saving time & paper.
Keyboard entry for patient ID information.
Capability to generate any number of ECG copies possible for filing & distribution.
Adult & pediatric analyzer programs std.
Automatic interpretation of ECG data.
Availability of adult, paediatric & neonatal accessories.
Optional accessories e.g. stand, cable, electrodes etc. should be quoted separately.
Consumable for one year.(a list should be attached) Service & operational manual complete.
SPECIFICATIONS PFT
• Flow Volume Measurement: =Spirometer
o Volume: 12 L
o Range: 0 to +/- 15 L/sec
o Accuracy: Better than 2% of scale
o Resistance: @ 10 L/sec < 5mm h1O
o Temperature: Internal spirometer thermistor
• DLCO Volume Measurement: Pneumotachograph
o Flow Range: 0 to +/- 20 L/sec
o Accuracy: Better than 2% of scale
o Resistance: @ 10 L/sec < 12mm h1O
o Pressure: Transducer Solid State
o Frequency: Response Flat to 50KhZ
o Pressure Range: 0 to +/- 100cm h1O
• Respiratory Pressures: Solid State Pressure Transducer
o Range: 0 to +/- 300 cm
• Helium Analyzer: Thermal Conductivity
o Range: 0 to 15.00% He
o Accuracy: +/- 1% (2 to 14% He)
o Response: Time Fixed to 30 seconds
o Oxygen: Compensation Automatic
• Carbon Monoxide Analyzer:
o Range: 0 to 0.500% CO
o Accuracy: +/- 2% (0 to 0.300% CO)
o Response: Fixed to 30 seconds
• Oxygen Analyzer
o Range: 0 to 100% O2
o Accuracy :+/- 1% (0 to 100% O2)
o Response Time: Fixed to 30 seconds
• Computer Requirements: Minimal Specifications
o Speed: 2 GHZ or faster
o RAM: 512 MB
o Hard Disk: 80 GB
o Operating system: latest configuration
o Printer: Any Windows® compatible
• Dimensions Unit
o Spirometer & main chassis
o Patient Valve Arm: 26" vertical adjustment
o Power: Single plug 110v
• Gas Requirements Single Cylinder
o DLCO Gas: Standard DLCO mixture (0.300% CO, 10.0% He, 21.0% O2 balance
N2)
• Lung Volume Gases 100% Helium and 100% Oxygen
o All regulator outputs: 50 psi
TECHNICAL SPECIFICATION OF ICU VENTILATOR
1. Microprocessor Control suitable for Paediatric and adult ventilation.
2. Electromagnetic Compatibility Hinged arm holder for holding the circuit.
3. Should have built in touch screen TFT display of 10”or more for display of waveforms
and Monitored value.
4. Facility to Measure and display:-
a) Status indicator for ventilator mode.
b) Battery life.
c) 3 wave-pressure & time, volume & time. flow & time.
d) Alarm setting.
5. Automatic compliance and leakage compensation for circuit and ET Tube.
6. Should have facility of log book, for events and alarms with date & time.
7. Should have following settings.
a) Tidal volume (Minimum at least 100ml, Maximum up to 2000ml)
b) Inspiratory Pressure (Up to 80 cm of H2O)
c) Respiratory rate 1 to 80 bpm.
d) SIMV Respiratory rate.
e) CPAP/PEEP
f) Pressure support.
g) Fi02
h) Pause Time
i) Pressure & flow Trigger
j) Inspiratory flow up to 120 Lpm.
8. Monitoring and Display of the following Parameters including Respiratory Mechanics.
a) Airway Pressure (Peak & Mean).
b) Tidal volume (Inspired & Expired).
c) Minute volume(Inspired & Expired)
d) Spontaneous Minute Volume.
e) Total Frequency.
f) F102 dynamic.
g) Intrinsic PEEP.
h) Plateau Pressure.
i) Resistance & compliance (Dynamic & Static).
j) Use selector Alarms for all measured & monitored parameters.
k) Occlusion Pressure.
l) Pressure Flow & Volume curves.
9. Modes of Ventilation:-
a) Assist I control
b) Volume controlled
c) Pressure Controlled
d) Pressure support
e) SIMV with pressure support (Pressure and volume control).
f) CPAP/PEEP
g) Inverse ratio Ventilation.
h) Non-Invasive ventilation
i) Airway pressure release ventilation (APRV).
j) Apnea Ventilation, User selectable, volume & pressure control.
k) Expiratory block should be autoclavable.
10. Should have built in alarms for Airway Pressure High & low , Minute volume, High &
low, power failure, Low oxygen, High Respiratory Rate, Air Source in Operable.
11 Medical Air Compressor:-
a) Noiseless, Rotary Type.
b) Of the same company as that of Ventilator to provide oil free Medical Air.
c) Air quality should comply with ISO compressed air purity class.
d) Internal (inbuilt) OR External (if external mounted on trolley)
12. Humidifier
a) Servo controlled heated Respiratory Humidifier
b) Temperature of delivered Gas on LED display
c) Temperature should be adjustable
d) In built Nebulizer
13 Should be supplied with following accessories:-
a) Reusable silicon patient circuit, Adult-1 no.
b) Reusable silicon Patient circuit, Paed-1 no.
c) Trolley with hinged arm.
d) HME Filters-50 nos.
e) Air & 02 hoses.
f) Good fitting Nasal Non-Invasive Ventilation Autoclavable mask of all sizes.
14 Battery Back-Up for 30 min.
15 CE / FDA Approval.
16 Demonstration of quoted model is a must
17 IMPORTED
18 Warranty / Guarantee: Minimum Two Years
PULMONARY DEPARTMENT
BLOOD GAS ANALYSER
A fully automated pH/Blood gas/electrolyte analyzer measuring the following parameters: -
pH, PCO2, PO2, Barometric pressure.
Na, K, Ca, Cl
Co-oximetry: ct Hb, CCO Hb, Met Hb, Sylf Hb, Haematocrit and Barometric pressure.
Sample volume should be approximate 100 μl for all parameters.
All calibration and cleaning cycles should be fully automated with user selectable
calibration items.
Calibration should be performed by liquid calibration for all parameters.
The electrodes provided should be zero maintenance including the reference electrode.
The system should have on board data manager to store all patient results, QC data and
calibrations.
The system should have a closed waste system and mentioned continuously. Also all the system
reagents should be monitored continuously.
A power fail protection for 20 min.to take all calibration and programmed data.
The analyzer should have a colour LCD screen to access all the system software and to display
the patient’s results. With alphanumeric key board/touch screen.
A built in printer should be provided to print out patient results.
The system should work in discrete testing, ie, selectable parameter testing.
Should be supplied with consumable, reagents and QC agents for 1000 tests, as per the user
requirements so that they do not expire.
Should not preferably use special gases.
BODY PLETHYSMOGRAPHY
Measured Parameters should be as follows
Complete Whole-Body Plethysmographic system for the measurement of:
Airway Resistance: Rtot, Reff, R0.5,..
Spec. Airway Resistance: sRtot, sReff, sR0.5,...
Static Lung Volumes: VC, ITGV, RV, ERV, IC, IRV, TLC, IVC, EVC, VCmax, RV/TLC,...
Dynamic Lung Volumes: FVC, FEV1, FEV1/FVC%, FEV1/VC%, ...
Maximal Flows: PEF, FEF75, FEF50, FEF25, FEF25-75%, ...
Components should be as follows
Airtight box, panorama glazing, with integrated intercom system and compensation vessel
Heated “High Quality“ pneumotach
Branded PC, printer and monitor
Set of accessories including a 3-liter calibration pump
Complete software for measurement and evaluation including powerful data management tool,
calibration programs and report generator
GDT interface for practice coupling; self-installation
Technical details are as follows:
Flow measurement: Pneumotach
Volume determination: Digital Integration
Mouth Pressure measurement: Peizoresistive
Box Pressure measurement: Peizoresistive
Box: Aluminium/acrylic
Calibration: Automatic
SPECIFICATIONS PFT SYSTEM WITH DIFFUSION STUDY
For the measurement of :
* Spirometry & Flow Volume Parameters,
* Maximum Ventilation Volume (MVV),
* Lung Volume & Sub-division, including TLC, RV & FRC by Multibreath
as well as Single Breath Helium Dilution Method,
* Single Breath Diffusion Capacity of Lungs (DLCO-He) ,Va, KCO,
* Respiratory Muscle Screening – MIP/MEP measurements,
* Pre & Post Bronchodilator Test.
System should have highest accuracy & reproducibility.
Volume Range : 0-12 Litre
Volume Resolution : < 8ml.
Minimum Flow Range : + 14 Litres/Sec (Linear)
Accuracy : < 3%
(Should meet Criteria for ATS Standards),
The system should incorporate heated Pneumotach + Dry Rolling Spirometer.
Should have Linear Gas Analyzers for :
Helium Analyzer, Range 0-15% Helium, Accuracy + 0.15%.
Carbon Monoxide Analyzer, Range 0-0.350% CO, Accuracy + 0.15%,
Should have O2 Analyzer for Precise O2 Compensation during FRC Test.
Oxygen Analyzer, Range 0-100% O2, Accuracy + 0.15%,
Should incorporate Electronic Barometric & Temperature Sensors for automatic BTPS
Correction.
Automatic Gas Control Module with Automatic Filling Circuit and Oxygen
Compensation.
Fully Automatic Test Procedure. Rapid & accurate Calibration with quality control.
System should incorporate easily removable Mouthpiece Assembly for rapid Cleaning
and Sterilization.
Should be supplied complete with Computer Interface, Cables, Trolley, PFT Software,
3 Litre Calibration Syringe, Standard accessories & Instructions Manual.
Gas Mixture Cylinders - Diffusion Gas Mixture (CO & He) – 2 Nos. & 100% He
Cylinder (1 No.) for FRC Test.
Additional Accessories : Pneumotach Screens (10 Nos), Pulmonary Filters (100 Nos), &
Expired Bags (5 Nos).
Latest Computer and Software.
CSSD
SPECIFICATIONS OF HIGH PRESSURE AUTOCLAVE
1. Chamber size 600 x 900 x 1500 mm. Capacity at least 850 liter, electric load of
36 Kw for heater +5 Kw for vacuum
2. Should be ISI/BIS marked as per IS: 3829
3. Should be double door, steam jacketed, suitable for operation on electricity
4. Chamber should be hydraulically tested to two times the working pressure
5. Normal working pressure should be 1.2 kg/cm2 at 121 c and 2.1 kg/cm2 at 134 c
6. Should have water ring vacuum pump to create vacuum for evacuation of the air
from chamber.
7. Chambers and doors would be of SS A ISI 316 quality.
8. Door should be provided with gasket
9. Chamber should be covered with glass wool insulation & cladded with painted
steel sheet.
10. Door should be on a hinge for self alignment
11. Door should have one automatic & one manual lock.
12. The automatic lock would operate at pressure in chamber of 0.37 Kg/cm2
13. The unit should be fully automatic with at least 5 preselected programs including
bowik test & leak test.
14. Should have 2 mechanical ejectors
15. Should have self sterilizing vacuum drier
16. Should have safety valve spring loaded & vacuum breaker
17. Should have pressure gauge
18. Should have dial thermometer & screen plug for chamber discharge live
19. Should have chamber discharge live with steam trap & swing check valve
20. Should have SS electric boiler under the shell with interconnecting steam pipes,
the boiler should have 36 Kw immersion heaters mounted on SS plate & electric
control would comprise of air break contractor, pressure controller, low water
protection with two neon indicators
21. The boiler should have gauge glass assembly with glass tube with protector,
water drain & water inlet valves.
22. The unit should be micro processor controlled for controlling entire cycle of
sterilization & steam pulsing automatically through water ring vacuum pump.
23. The control panel should have automatic pressure control arrangement for
timers, relay, and contactors.
24. The digital display at front panel should show the following parameter
• Chamber pressure
• Chamber temp.
• Cycle no.
• Batch no.
• Time & date
• Alarm indicator
• Low water indicator
• Time elapsed after start of cycle
25. Printer-to automatically & continuously monitor & record dates ,time of day,
load, identification No. and operating parameters like temp., pressure through out
the length of autoclave cycle
26. The unit should be provided with following :
• SS loading /unloading carriage-one
• MS tubular transfer trolley-Two
DERMATOLOGY DEPARTMENT
SPECIFICATION OF FOLLOWING EQUIPMENTS/INSTRUMENTS OF
DERMATOLOGY DEPARTMENT
1. COMPOUND LIGHT MICROSCOPE
• Eyepiece Lens: 10X or 15X power.
• Binocular Head: Inclined 30°, rotatable 360°, Interpupilary distance 55-
75mm
• Illuminator: A steady light source (110 volts)
• Stage: Mechanical stage with Stage clips to hold the slides in place.
• Revolving Nosepiece or Turret
• Objective Lenses: of 4X, 10X, 40X and 100X (oil immersion) powers.
• Condenser Lens: N.A. 1.25
• Diaphragm or Iris
2. DARK FIELD MICROSCOPE
• Eyepiece Lens: 10X or 15X power.
• Binocular Head: Inclined 30°, rotatable 360°, Interpupilary distance 55-
75mm
• Illuminator: A steady light source (110 volts)
• Stage: Mechanical stage with Stage clips to hold the slides in place.
• Revolving Nosepiece or Turret
• Objective Lenses: Of 4X, 10X, 40X and 100X powers.
• Dark field condenser
• Condenser Lens: N.A. 1.25
• Diaphragm or Iris
3. LIQUID NITROGEN CRYOJET MACHINE
• Cryojet nitrogen jet and stand with different types of nozzle tips.
• Shield flow unit
• 75 litre nitrogen storage tank
• Temperature range 90 to 300 K
• Temperature stability ±0.1 K
• Gas flow range 0 to 10 l/min
• Liquid nitrogen storage tank hold time atleast 65 hours
4. PUVA CHAMBER
• Phototherapy chamber of 18 UVA and 18 NBUVB tubes
• UV chokes and cooling fans
• Integrated Dosimeter system
• CE or FDA or ISI certification
• Advanced micro computerised LCD/TFT controller
• Automatic computation of Irradiation time from joules input
• Provision of data storage and software back up
• UVA/NBUVB sensors
• Automatic switch off and warning alarm at the end of session
• Built in memory
• Rust free body metal
• Automated and /or mechanical safety mechanism to prevent excess irradiation
• Electrical leakage circuit breaker /tripper
• Open top unit
• Mechanism to provide duration of treatment and time left for exposure
• Computer for patient data management with software & interface for phototherapy
chamber which is RS 232 compatible
• Stabiliser
• Warranty period 2 years
• Black UV goggles with eye pads( 3 pairs for adults;3 pairs for children)
5. WOODS LAMP
• Special fluorescent bulbs emitting UVA at approximately 360 nm wavelength
• Provision of minimum 1 white bulbs and 1 UV bulbs with bulb life of minimum 5,000
hours
• Optically ground and polished glass 5 diopter magnifier lens with magnification with
appropriate focal length
• Portable, hand-held lights for maximum flexibility
• Appropriate voltage and wattage as per standards
6. TATTOO MACHINE
• Stainless Steel tattoo machine/Pencil with Input 100-240 V , Output 3-18 Vand clip
cord&foot switch
• Tattoo Ink
Tattoo Ink Volume 4 × 5ml
Color : Bright Red, Dark Brown, Light Green, Light Purple
• Tattoo Needles (preferably disposable) 20 pieces. Type: 5 x tattoo needle RL 3, 5 x tattoo
needle RL 5, 5 x tattoo needle RS 5, 5 x tattoo needle RS 3
• Tattoo Tip: 10 x stainless steel tip, 10 x disposable tip
Other Accessories (optional) at least
Carrying Case 1
Tattoo Ink Cup (Pcs) 100
Tattoo Ink Cup Holder (Pcs) 1
Tattoo Transfer Paper (Pcs) 1
Practice Skin (Pcs) 1
Rubber Band (Pcs) 50
O Ring (Pcs) 50
Needle Grommet (Pcs) 50
DENTAL DEPARTMENT
SPECIFICATION OF COMPLETE DENTAL UNIT
Doctors element with flexible positioning easy adjust six different functions for hand piece.
1. Syringe,water(hot and cold)/air(1)
2. Turbine, air driven (1)
3. Drill, electrical with fiber optic light(3)
4. Electrosurgical unit with fibre optic light (1)
5. Ultrasonic scaler (1)
6. UV light (1)
7. Five positions element ,including syringe control and foot control for unit functions and
chair movements.
8. Assistants element with flexible positioning , easy adjustable
SUPPORTING FIVE DIFFERENT FUNCTIONS
1. Syringe (1)
2. Curing light (2)
3. High suction (1)
4. Salive Ejector (1)
5. Saliva flushing device with safety valve
Cuspidor
1. Scratch resistant bowl
2. Integrated sterilized water system, tempered with filter
3. Instrument tray supporting including 10 pcs , stainless steel trays
DENTAL CHAIR
Full positioning programme from sitting to flat horizontal and trendelenberg position.
Specifications
1. Electrically adjustable preprogrammable positioning
2. Backrest, seat, leg supporting foot and hand control, easy operated and easy accessible
3. Armrest(90degree horizontal turnable) and head support manually or electrically adjustable
4. All sections upholstered and covered with material easy to clean and disinfect.
SUCTION UNIT
Compact design suction unit for saliva ejectors and dental suction equipment
1. Built in noise suppressors
2. Negative pressure limitation
3. Compressor, low noise , for bone dental unit
4. Compressor unit for hygienic ,impeccable air production
5. Multipurpose spray and cooling sprays of the drills
6. Oil free running
7. Noise suppression (max,level 70dB),vibration insulation
Air container capacity atleast 20 L
Air delivery capacity atleast 50L/min
Cut in pressure 5.5 bar
Cut out pressure 7.0 bar
CHEST, INSTRUMENT, MOBILE
1. Chest of drawers for dental instruments, with castors minimum four drawers
2. Drawer fronts and chest top to be manufacture from 18 mm thick plywood, laminated with
0.9mm melamine and lipped with 3mm thick PVC lipping
3. Drawers to be fitted with steel sheet sides, epoxy coated or robust plastic construction and slide
runners with nylon gliders.
4. Vertical treatment cabinet for doctor and sister
5. To be from same source as the slipper of dental unit.
6. Working stool for doctor and assistant with backrest and footing
7. Seat and backrest fully adjusted
8. Upholster seat and backrest
9. Upholstery, polythane foam or similar, covered with plastic coated elastic fabric, antibacterial,
flame hardened and topical heat resistant.
10. Robust Frame construction, non corrosive material or treatment five star base with castors.
DENTAL X-RAY (IOPA-X-RAY)
Simultaneous ignition, mAs system
Rated Peak tune potential and rated tube current 70kv Vp 10 mA
Total Filtration 2.1 mm Al
Oil Cooling System
S.S.D. 200M
Hand Switch
DENTAL AUTOMATIC FILM PROCESSOR
Fully automatic film processor with an integrated chemical replenishment system with infrared
sensors for optimal chemical condition complete with daylight loader, film box 8X10 and 6X12,
240V50Hz. Unit should be complete with stand or table for mounting the unit and film cassette.
INTRA ORAL DIGITAL RADIOGRAPHY
- Unit for Digital intra oral radiography
- Wall mounted flexible suspension.
- System, easy adjustment and polishing
COPMRISING
- Tube Head
- Control Unit
- Suspension system
- X-ray Sensor, CCD
- Lap-Top
FUNCTIONS/SPECIFICATION
(Tube head)
- 70 Kv, Multi – pulse 10 Ma
- Focus spot : 0.8x0.8 mm
- Focus-Skin Distance : 200mm AL
- Radiated field at end of cone : Diameter =60mm
- Total Filter : min 2.1 mm AL
CONTROL UNIT
- Exposure release control, L (cable) min:3 m
- Exposure time setting, range min. 0.005-3.2 sec
SUSPENSION UNIT
- Manoeuvaranbility
- Vertical min 270 degrees
- Horizontal 360 degrees
To be supplied with:
1 pack of sensor covers, 100 pcs.
LAP-TOP
- I-7
- RAM – 4GB
- Hard Disc – 500 GB
- 14.1 inch
- Window 8