TELEMEDICINE EQUIPMENT SPECIFICATION

1. COMPUTERIZED ECG MACHINE (12 CHANNEL) (Adult & Pediatric)

1. Should be a 12 Leads ECG simultaneous acquisition system for adult &
Pediatric.
2. The system should have a digital signal processor, to get higher quality ECG
waveforms through the AC filter, baseline filter and EMG filter of the ECG
signals
3. Should have a foldable LCD indicating working status, waveforms, leads off
and other selections like paper speed. Muscle filter etc.
4. Should work based on Resting Interpretation Algorithm.
5. The equipment should be able to interface with system for transmission and
storage purposes for reference.
6. I/O Communication - COM1 - RS 232 & VGA O/P.
7. Should be a portable system
8. Accessories and Consumables to be supplied:
i. ECG Leads
ii. Electrodes
iii. Contact jelly
iv. 6 nos. Of 30 meter rolls ECG recording paper
9. Should have an integrated thermal array printer for A4 size print out of ECGs.
10. Standard Leads acquired I, II, III, aVR, aVL, aVF, V1, V2, V3, V4, V5, V6.
11. Pediatric/Newborn limb and chest leads should be ½ an inch diameter
12. Input Impedance, Input Dynamic Range, Electrode Offset tolerance and
Common Mode Rejection to meet or exceed requirements of ANSI/ AAMI EC
11
13. Patient Leakage Current, Chassis Leakage Current to meet or exceed
requirements of ANSI / AAMI ES1
14. Digital Sampling Rate: 2,000 s/sec/ per electrode/lead.
15. Equipment should have at least 24-bit A/D conversion provides 5µV
resolution.
16. Should have basic controls like on/standby, auto-manual, chart speed, ECG
size, copy, filter, page advance etc.
17. Thermal recorder: Computer controlled dot array or equivalent.
18. Should have a memory option to store minimum 100 ECGs which are
retrievable.
19. Thermal Writer Speeds 12.5, 25, or 50 mm/sec.
20. Gain Settings. 5, 10, or 20 mm/mV.
21. Report print formats: Standard or Cabrera: 3 x 4 with 1 Rhythm or 6 x 2
Cabrera, Rhythm (3 and 6 pre-set lead selections).
22. Rhythm Print Format: 3 Channels, 6 Channels.
23. Frequency response 0.05Hz to 150 Hz.
24. Filters: Baseline Filter, AC Interference Filter 50Hz, Low Pass Filters 40 Hz,
or 150 Hz.
25. Should have CMRR of 110 dB or greater.
26. Should have input impedance greater than 15Mohms.
27. Should perform a self test each time the cardiograph is turned on.
28. Device Classification: Class I / Class II Type CF defibrillation proof
29. Power 220-240 V 50 Hz.
30. Internally Rechargeable Lithium ion Battery with long duration of battery
operation of at least 30 ECG’s or 30 minutes of continuous monitoring in a
discharge.
31. The instrument should have the function of regular auto-analysis and auto-
interpretation of ECG waveform parameter, and provide measurement
parameters such as HR, P-R interval, P Duration, QRS Duration, T Duration,
Q-T interval, Q-Tc, P Axis, QRS Axis, T Axis, etc and should provide auto-
interpretation conclusion.
32. Equipment should be provided with a Trolley and cable hangers.
33. The equipment should be suitable for operation in temperatures from 10 0 C
to 450 C with a relative humidity of 100%
34. Equipment offered shall be adequately protected against and be able to
withstand the prevailing climate in Tamil Nadu.
35. Equipment should be provided with a line cord (power cord) of acceptable
durability, quality, length and current carrying capacity.
36. Equipment should include power plugs that are sufficient for maximum
voltage and current of the equipment.
37. If fuses are used, a spare fuse should be provided Permanent marking near
each fuse holder should indicate fuse ratings.
 38. Equipment sensitive to fluctuations should be provided with stabilizers.
39. Equipment performance should not be affected by electromagnetic
interference radiated or conducted through power lines from another device.
40. Equipment should have no sharp edges, should be securely mounted and
should provide adequate protection against moving and electrically energized
parts.
41. Controls (e.g. switches knobs) should be visible and clearly identified.
42. Labels and markings should be clear and visible.
43. Equipment should be simple to use, operate and maintain. It should be
designed for easy access to serviceable parts.
44. Equipment should include a soft/ hard carrying case and Study questions,
Dos and Don’ts, instructions manual, maintenance guide, background
information, User manual with trouble shooting guidance, technical manual
with maintenance and first line technical intervention instructions and any
other relevant teaching/ training materials in English.
45. Equipment should have detailed information of the device features,
functions, detection capabilities, method of operation, materials, alarm
capabilities, software, specifications and operating ranges, power source,
parameter detection ranges, etc. wherever applicable.
46. The supplier/ manufacturer should list the name and address of both
Regional and Head office technical service providers in India
47. The supplier must ensure the availability of on call service agreement from
state headquarters within 48 hours, from local within 24 hours, from outside
state within 7 days and in case the problem is not rectified on site at the
time of service then its need to be rectified within next 7 days for minor
defects and within 28 days for major defects.
48. Packaging and Storage
a) Packing of the equipment should be easy to open and well labeled and
marked with devices name and sellers name and address.
b) Equipment should be able to withstand temperature and humidity
extremes likely to be encountered during storage and transportation
49. Equipment should conform to the equivalent Indian Standard or other
equivalent international or third country standard for good manufacturing
practice and safety.
50. Bidders may please indicate standard(s) with which the product complies and
should provide evidence of compliance. Alternately bidders may indicate that
their device is registered with national or international medical devices
regulation agencies such as USFDA or EUMDD which assures that the
product meets GMP, performance and safety standards.
 2. PULSE OXIMETER
Technical specifications:
1. The unit should be Microprocessor controlled, compact and fully portable to
determine non-invasive measurement, the percentage oxygen saturation of
hemoglobin in the arterial blood.
2. The unit should provide a plethysmographic (waveform) display proportional
to signal strength.
3. It should be small light weight for easy portability.
4. It should have backlit LCD display for easy viewing of the waveform even in
the dark condition and large LED display for digital read-out of SpO 2 & pulse
Rate values.
5. The system should be easy to use and effective on patient, from neonates to
adults.
6. SpO2 and pulse rate displays, alarm: low SpO2, high SpO2, low pulse, high
pulse, (easily adjustable from front panel) diagnostic routines to aid in-house
servicing.
7. Unit should have built in software for artifact correction, stable display &
accurate recording even if patient is moving.
8. The unit should have built-in battery backup.
9. The unit should have a red alert bar to warn of alert conditions if audio is
turned off.
10. The pitch of pulse should vary with SpO2 value.
11. Technical Specifications:
a) Pulse rate range 30 - 250 beats per minute with accuracy ±2 beats per
minute
b) SpO2 range 20 to 100% with accuracy ±2% (for 80-100% SpO2)
c) Alarm limit range Low SpO2 50-100%; High SpO2 70 - 100%
d) Alarm Limit: Low pulse 40 - 200 beats per minute. High pulse 70 - 250
beats per minute.
e) Operating temperature 10° C to 40o C; Humidity: 0 to 90 % relative.
f) Power Source : 190-260 V, 50Hz, Single phase (5 Amps)
12. Unit should conform to BIS 11753 standard or equivalent.
 13. Equipment offered shall be adequately protected against and be able to
withstand the prevailing climate in Tamil Nadu.
14. Equipment should be provided with a line cord (power cord) of acceptable
durability, quality, length and current carrying capacity.
15. Equipment should include power plugs of having 3 pins (Line, Neutral and
Earth) and compatible with standard style/design of socket.
16. If fuses are used, a spare fuse should be provided; permanent marking near
each fuse holder should indicate fuse ratings.
17. Equipment performance should not be affected by electromagnetic
interference radiated or conducted through power lines from another device.
18. Equipment should have no sharp edges, should be securely mounted and
should provide adequate protection against moving and electrically energized
parts.
19. Controls (e.g. switches, knobs) should be visible and clearly identified.
20. Labels and markings should be clear and visible.
21. Equipment should be simple to use, operate and maintain. It should be
designed for easy access to serviceable parts.
22. Packaging and Storage
 Packing of the equipment should be easy to open and well labeled and
marked with devices name and sellers name and address.
 Equipment should be able to withstand temperature and humidity
extremes likely to be encountered during storage and transportation.
23. Equipment should conform to the equivalent Indian Standard or other
equivalent international or third country standard for good manufacturing
practice and safety.
24. Bidders may please indicate standard(s) with which the product complies
and should provide evidence of compliance. Alternately bidders may indicate
that their device is registered with national or international medical devices
regulation agencies such as USFDA or EUMDD which assures that the
product meets GMP, performance and safety standards.
25. Alarms: Audio visual alarm in case of measurement /outside preset range.
a) Silencing features for audio alarm.
26. Should display report system error, leads, sensor failure & built-in battery
status.
27. Should work on mains (220 V/ 50 Hz) and Battery.
28. Should have min. 3-hrs battery backup.
29. Should automatically switch from mains to battery in case of power failure.
30. Monitor should be constructed of shock proof material.
31. Standards:
a) CE / FDA Approved
b) IEC 60601-1 Certified
c) UL 2601-1 Classified
32. Scope of supply must include:
a) Compact, portable, unit with battery for all patients (paediatric &
neonates)
b) One spare rechargeable battery.
c) SpO2 finger sensor probe( paediatric, neonate)
d) Reusable SPO2 neonate clips-on type sensor – 2 nos.
e) Reusable SPO2 neonate wrap around type sensor-2 nos.
f) Mountings (Arms, Plates) for the equipment
g) One spare fuse.
h) User manual
33. Equipment should include a soft/ hard carrying case and Study questions,
Dos and Don’ts, instructions manual, maintenance guide, background
information, User manual with trouble shooting guidance, technical manual
with maintenance and first line technical intervention instructions and any
other relevant teaching/ training materials in English.
34. Equipment should have detailed information of the device features,
functions, detection capabilities, method of operation, materials, alarm
capabilities, software, specifications and operating ranges, power source,
parameter detection ranges, etc. wherever applicable.
35. The supplier/ manufacturer should list the name and address of both
Regional and Head office technical service providers in India
36. The supplier must ensure the availability of on call service agreement from
state headquarters within 48 hours, from local within 24 hours, from outside
state within 7 days and in case the problem is not rectified on site at the
time of service then its need to be rectified within next 7 days for minor
defects and within 28 days for major defects.
37. Packaging and Storage
a) Packing of the equipment should be easy to open and well labeled and
marked with devices name and seller’s name and address.
b) Equipment should be able to withstand temperature and humidity
extremes likely to be encountered during storage and transportation.
38. Equipment should conform to the equivalent Indian Standard or other
equivalent international or third country standard for good manufacturing
practice and safety.
39. Bidders may please indicate standard(s) with which the product complies.
Alternately bidders may indicate that their device is registered with national
or international medical devices regulation agencies such as USFDA or
EUMDD, which assures that the product, meets GMP, performance and
safety standards.
 3. MULTI PARAMETER MONITOR
GENERAL
1. The equipment should be microprocessor based and fully controlled by
software
2. Should be able to interface with system for storage and digital communication
purposes for reference
3. DISPLAY PARAMETERS -
a) ECG (5 lead, i.e. RA, LA, RL, LL, V)
b) SPO2
c) NIBP
d) RESPIRATION
e) TEMP.
2. DISPLAY SIZE- Not less than 10 inch colour TFT SCREEN with a
resolution not less than 800 x 600-pixels
3. WAVE FORM - Not less than 4 waveforms.
4. TREND - 72 hours numeric and graphic for all parameters.
5. POWER INPUT - 230 V ±10%, 50 Hz.
6. BATTERY - Should have a built in rechargeable battery with a back up
time of 2 hours
7. POWER CONSUMPTION -less than 50 Watts.
8. ALARM LIMITS- HIGH - LOW Alarm Limits for all Parameters with mute
facility.
9. WEIGHT - Less than 4.5 kg and easily portable
10. I/O Communication - COM1 - RS 232 & VGA O/P.
11. Systems should be able to upgrade to EtCO2 & Printer in future
ECG
1. CHANNEL - 2 Channels.
2. LEADS - 3 / 5 Lead ECG (I, II, III, / aVR, aVL, aVF, V). Selective
3. HEART RATE - 20 to 270 BPM ±3 - 5 %
4. GAIN - Auto Gain or Selectable.
5. RESPIRATION - ECG Lead LA-RA Impedance Method
RR Rate 2-150 BPM ±1%
6. Should have defibrillator/ESU protection, pacemaker detection, ST Level
measurement and arrhythmia analysis.
SpO2
1. RANGE - 0 to 100%
4. ACCURACY - ±2% for 70% - 100%
±3% for 50% - 70%
5. System should have built in software for artifact correction, stable display,
low Perfusion and patient moving and with plethysmograph form.
NIBP
1. METHOD - Oscillometric_
2. DISPLAY - SYSTOLIC, DIASTOLIC and Mean Pressure with High -Low
Alarm Limits.
3. MEASUREMENT RANGE - 20 to 250 mm mercury.
4. MODES - Manual, Continuous (STAT) and user selective
(3minutes - 60 minutes)
TEMPERATURE (CORE & SKIN)
1. SENSOR - THERMISTER (or) Equivalent
2. ACCURACY - ±2° C
3. MEASUREMENT RANGE - 0° to 50 °C
4. RESOLUTION - 0.1OC
RESPIRATION:
1. RANGE : 0-80 bpm (adult) and 0-80 (pediatric/neonate)
2. ACCURACY : ±2 bpm
3. RESOLUTION :1 bpm
4. Should have APNEA alarm with a delay of 10-40 sec.
ACCESSORIES:
1. One additional set of all accessories (ECG cable,SPO2 probe, NIBP cuff,
Thermister sensors for temperature and respiration parameter measurement)
2. 3 / 5 Lead ECG Reusable Cable (Suitable for Adult & neon natal)
3. Spo2 Finger Reusable rubberized Probes Adult-1 & Neonatal - Y Probe
4. NIBP Cuff - 5 Nos (Adult (Large, Medium, Small), Neonatal-2 Sizes)
5. NIBP Hose -minimum 3 meters
6. Electrodes: FOR ECG - 100 Nos.(Disposable for adult and Neonatal)
7. Temperatrure: Skin temperature probe
OTHER REQUIREMENTS
1. Should have memory storage capacity of at least 200 NIBP measurements,
50-alarm events storage with full disclosure of ECG.
2. The equipment should be suitable for operation in temperatures from 100 C
to 450 C with a relative humidity of 100%
3. Equipment offered shall be adequately protected against and be able to
withstand the prevailing climate in Tamil Nadu.
4. Equipment should be provided with a line cord (power cord) of acceptable
durability, quality, length and current carrying capacity.
5. Equipment should include power plugs that are sufficient for maximum
voltage and current of the equipment.
6. If fuses are used, a spare fuse should be provided. Permanent marking near
each fuse holder should indicate fuse ratings.
7. Should provide Mountings (Arms, Plates) for Monitor
8. Equipment sensitive to fluctuations should be provided with stabilizers.
9. Equipment performance should not be affected by defibrillation,
electromagnetic and electrosurgical interference radiated or conducted
through power lines from another device.
10. Equipment should have no sharp edges, should be securely mounted and
should provide adequate protection against moving and electrically energized
parts.
11. Controls (e.g. switches knobs) should be visible and clearly identified.
12. Labels and markings should be clear and visible.
13. Equipment should be simple to use, operate and maintain. It should be
designed for easy access to serviceable parts.
14. Equipment should include a soft/ hard carrying case and Study questions,
Dos and Don’ts, instructions manual, maintenance guide, background
information, User manual with trouble shooting guidance, technical manual
with maintenance and first line technical intervention instructions and any
other relevant teaching/ training materials in English.
15. Equipment should have detailed information of the device features,
functions, detection capabilities, method of operation, materials, alarm
 capabilities, software, specifications and operating ranges, power source,
parameter detection ranges, etc. wherever applicable.
16. The supplier/ manufacturer should list the name and address of both
Regional and Head office technical service providers in India
17. The supplier must ensure the availability of on call service agreement from
state headquarters within 48 hours, from local within 24 hours, from outside
state within 7 days and in case the problem is not rectified on site at the
time of service then its need to be rectified within next 7 days for minor
defects and within 28 days for major defects.
18. Packaging and Storage
c) Packing of the equipment should be easy to open and well labeled and
marked with devices name and seller’s name and address.
d) Equipment should be able to withstand temperature and humidity
extremes likely to be encountered during storage and transportation.
15. Equipment should conform to the equivalent Indian Standard or other
equivalent international or third country standard for good manufacturing
practice and safety.
16. Bidders may please indicate standard(s) with which the product complies.
Alternately bidders may indicate that their device is registered with national
or international medical devices regulation agencies such as USFDA or
EUMDD, which assures that the product, meets GMP, performance and
safety standards.
 3. ELECTRONIC STETHOSCOPE
Electronic stethoscope to measure heart sound and lung sounds with the
following specifications:
1. Display: High resolution LED with graphical display for heart sounds and
lung sounds
2. Equipment should be able to provide visual representation of heart sounds
and interpret murmurs
3. Electrical specifications:
i) Should work on 5 V DC power supply
ii) Rechargeable Li- ion 3. 7 V internal battery
iii) Supplied with Medical grade charger
input: 230 V AC, 50/60 Hz
output: 5 V DC, 1000mA
iv) Equipment should work for more than 7 hours continuously
4. Switches and Controls:
i) Switch for turning equipment ON and OFF
ii) Switch for recording heart sound
iii) Switch for changing mode from heart sound to lung sound
iv) Control to adjust volume
v) Control to freeze waveform
5. Equipment should be supplied with data cord for transmitting data to the
system. Same data cord shall also be used for charging the device.
6. Equipment should be supplied with:
i) Installation software
ii) User manual
iii) Phonocardiogram
iv) Spare set of ear pieces- 2 sets
v) Spare diaphragm
7. Equipment should be Class II type device working o internal battery
8. The device should be biocompatible type as per ANSI/ AAMI/ ISO 10993
9. Equipment should not weight more than 250 g (including battery placed
inside)
 19. Equipment performance should not be affected by defibrillation,
electromagnetic and electrosurgical interference radiated or conducted
through power lines from another device.
20. Equipment should have no sharp edges, should be securely mounted and
should provide adequate protection against moving and electrically energized
parts.
21. Controls (e.g. switches knobs) should be visible and clearly identified.
22. Labels and markings should be clear and visible.
23. Equipment should be simple to use, operate and maintain. It should be
designed for easy access to serviceable parts.
24. Equipment should include a soft/ hard carrying case and Study questions,
Dos and Don’ts, instructions manual, maintenance guide, background
information, User manual with trouble shooting guidance, technical manual
with maintenance and first line technical intervention instructions and any
other relevant teaching/ training materials in English.
25. Equipment should have detailed information of the device features,
functions, detection capabilities, method of operation, materials, alarm
capabilities, software, specifications and operating ranges, power source,
parameter detection ranges, etc. wherever applicable.
26. The supplier/ manufacturer should list the name and address of both
Regional and Head office technical service providers in India
27. The supplier must ensure the availability of on call service agreement from
state headquarters within 48 hours, from local within 24 hours, from outside
state within 7 days and in case the problem is not rectified on site at the
time of service then its need to be rectified within next 7 days for minor
defects and within 28 days for major defects.
28. Packaging and Storage
1. Packing of the equipment should be easy to open and well labeled and
marked with devices name and seller’s name and address.
2. Equipment should be able to withstand temperature and humidity
extremes likely to be encountered during storage and transportation.
15. Equipment should conform to the equivalent Indian Standard or other
equivalent international or third country standard for good manufacturing
practice and safety.
16. Bidders may please indicate standard(s) with which the product complies.
Alternately bidders may indicate that their device is registered with national
or international medical devices regulation agencies such as USFDA or
EUMDD, which assures that the product, meets GMP, performance and safety
standards.
17. The equipment should be suitable for operation in temperatures from 10 0 C
to 450 C with a relative humidity of 100%
18. Equipment offered shall be adequately protected against and be able to
withstand the prevailing climate in Tamil Nadu.
 4. STADIOMETER
Stadiometer with Measuring Tape:
1. Height measuring scale should be a placed on wall in which the patient can
Stand for measurement of height up to 200 cm
2. It should be a robust model for day to day rough use in wards and OPD.
3. It should measure the height in centimetre.
4. It should be portable to allow free mobility from one place to other.

5. WEIGHING MACHINE- ADULT

1. Strongly constructed machine of modern design made of Metallic Steel

material.
2. Revolving dial with a magnifying lens for easy reading of scale graduations.
3. Should incorporate shock absorbing mechanism for quick stabilization of
readings.
4. Should have a non – slip platform surface.
5. Weighing Scale range 0 to 150 kg with calibration interval of 0.1kg.
6. The model offered should be an approved one by the Weight and Measures
Dept., Govt. of India, under the provisions of Standards of Weights and
Measures Act.
7. The equipment should be suitable for operation in temperatures from 10 0 C
to 450 C with a relative humidity of 100%.
8. Labels and markings should be clear and visible.
 6. PORTABLE LAB KIT
The system should comprise the following
a. Analyser
b. Centrifuge
c. Micropipette
d. Micropipette tips
e. Incubator
f. Cuvette
g. Cuvette stand
General Requirements for the system:
7. Equipment performance should not be affected by defibrillation,
electromagnetic and electrosurgical interference radiated or conducted
through power lines from another device.
8. Equipment should have no sharp edges, should be securely mounted and
should provide adequate protection against moving and electrically energized
parts.
9. Controls (e.g. switches knobs) should be visible and clearly identified.
10. Labels and markings should be clear and visible.
11. Equipment should be simple to use, operate and maintain. It should be
designed for easy access to serviceable parts.
12. Equipment should include a soft/ hard carrying case and Study questions,
Dos and Don’ts, instructions manual, maintenance guide, background
information, User manual with trouble shooting guidance, technical manual
with maintenance and first line technical intervention instructions and any
other relevant teaching/ training materials in English.
13. Equipment should have detailed information of the device features,
functions, detection capabilities, method of operation, materials, alarm
capabilities, software, specifications and operating ranges, power source,
parameter detection ranges, etc. wherever applicable.
14. The supplier/ manufacturer should list the name and address of both
Regional and Head office technical service providers in India
15. The supplier must ensure the availability of on call service agreement from
state headquarters within 48 hours, from local within 24 hours, from outside
 state within 7 days and in case the problem is not rectified on site at the
time of service then its need to be rectified within next 7 days for minor
defects and within 28 days for major defects.
16. Packaging and Storage
 Packing of the equipment should be easy to open and well labeled and
marked with devices name and seller’s name and address.
 Equipment should be able to withstand temperature and humidity
extremes likely to be encountered during storage and transportation.
11. Equipment should conform to the equivalent Indian Standard or other
equivalent international or third country standard for good manufacturing
practice and safety.
12. Bidders may please indicate standard(s) with which the product complies.
Alternately bidders may indicate that their device is registered with national
or international medical devices regulation agencies such as USFDA or
EUMDD, which assures that the product, meets GMP, performance and
safety standards.
13. The equipment should be suitable for operation in temperatures from 10 0 C
to 450 C with a relative humidity of 100%
14. Equipment offered shall be adequately protected against and be able to
withstand the prevailing climate in Tamil Nadu.

ANALYSER
17. Portable Analyser to diagnose the following clinical parameters
a. Haemoglobin
b. Random blood sugar
c. Blood Urea
d. Serum Sodium
e. Serum Potassium
f. Total Protein
g. Serum Albumin
h. Bilirubin – Total + Direct
18. Modes: % Transmission and Absorbance modes
19. Photometric range 0.000 to 2.5 abs
20. Wavelength must cover 340 nm to 650 nm
 21. Silicon photodiode Photo detector system with LED light source
22. Aspiration and reading by cuvette with 10 mm path length cuvette based
Sample system
23. Sample volume- 5µl
24. Multi point calibration system
25. Flow cell temperature should be programmable at 250, 30, 37 C with tolerance as
0.1 (maximum); machine should not take more than 1 minute for reaching 25 to
37 C or 37 to 25 C
26. Machine must have user-friendly keyboard and operations with bright LCD
display.
27. Quality control program facility to be available.
28. Analyzer must have patients’ data storing capacity. At least 100 last results must
remain in memory.
29. Patient’s name and number (ID) printing options will be required.
30. Input power: 230 V AC ±10%, 50Hz
31. Machine should be supplied with internal printer.
32. USB port connectivity for interfacing the unit with system
33. The unit should be able to work with all standard reagents available in the
open market.

CENTRIFUGE
1. 6 bucket type with safety lid lock
2. Provision to adapt 0.2 ml and 0.5 ml tubes
3. Stepless speed control upto 6000 rpm
4. Electronic timer with Digital display of time and speed of rotation
5. Power supply: : 230 V AC ±10%, 50Hz

MICROPIPETTE
 5µl - 50 µl – 1 No
 100 µl – 1000 µl- 1-No
1. Calibration should satisfy the standards of ISO 8655 and ISO 17025.
Necessary certificates to be submitted by the manufacturer.
2. User friendly high performance air displacement pipettes with compression
spring mechanism.
3. Ergonomic Design With Light Pipetting Action. 9 N to 14 N force required for
pipetting
4. Durable tip cone materials made of PVDF plastic to provide excellent
chemical resistance.
5. Availability of servicing facility for the manufacturer & supplier to calibrate
the Micropipettes in accordance to NABL in India or equivalent to
International Standards.
6. Digital display clearly reads volume setting 
7. Ejector collar and tip cone can be removed for easy cleaning and
maintenance
8. Volume setting by click stops
9. Ease for on sight preventive maintenance and calibration
10. Supplied with full documentation warranty, Calibration certificate along with
tools for servicing and calibration
INCUBATOR
1. Incubator operating in the temperature range of 20°C to 45°C
2. Heating element: Mica
3. Controller: PID controller
4. Power supply: : 230 V AC ±10%, 50Hz

MICROPIPETTE TIPS

Microtips for Micropipettes with the following sample capacity

 5µl - 50 µl
 100 µl – 1000 µl

CUVETTES
Cuvette sample capacity of 2 ml

CUVETTE STAND
Cuvettes stand for holding a minimum of 100 cuvettes in 25 x 4 matrix