1.

Ultrasound-Doppler, Fetal Each 2

2. Glucometer with strip Each 35 Vital
3. Infusion-pump, Each 12
4. Sphygmomanometer-Aneroid, Adult/Ped./Infant Each 60 Vital
5. Sphygmomanometer-Digital, Adult/Ped./Infant Each 73 Vital
6. Stethoscope - Adult Each 70 Vital
7. Stethoscope - Neonatal Each 31 Vital
8. Pulse Oximeter Each 100 Vital
9. Steam sterilizer each 2
10. Otoscope each 3
11. . Wheel chair - Adult, Each 20 Vital
12. Couch - Examination, Gynaecological Each 8
13. IV Stand Each 300 Vital
14. Trolley - Patient Record Each 40
15. Crash cart trolly each 8
16. Delivery couch each 6
17. Patient bed side table with mediaction cabinate each 317
18. Patient monitor
19. Mobile light operating
Crash Chart (5 Locked Emergency medication cabinate) ??????

1. Technical specification for pulse oximeter

1. Generic name: Pulse oximeter
2. GMDN name: Pulse oximeter, battery-powered (handheld)
3. Quantity: 100 each
4. Feature
 Displays patient oxygen saturation and pulse rate in real time using an
external probe on the skin.
 Display and probe built into one case.
 Intended for time-limited spot checks, so alarm features not required.
 Operates from internal battery (locally available type, rechargeable or
non-rechargeable)
 Detailed requirements
o SpO2 measurement range at least 70 to 99 %, minimum
resolution 1%
 Accuracy of SpO2 better than ± 2%
 Pulse rate range at least 30 to 240 bpm, minimum gradation 1 bpm
 Accuracy of pulse rate better than ± 4 bpm
 Signal strength or quality to be visually displayed.
 Automatic power-off facility required after minimum of 1 minute.
 Low battery display required.
 Facility for data download preferred.
 Digital equipment with autocorrelation algorithm.
 Internal memory continuous data storage time not less than 12 hours.
5. Displayed parameters.
Integrated display for data visualization with size not less than 5 inches.
Video display of at least the following parameters:
a) SpO2 sensor connected.
b) alarms disabled.
c) low battery life.
 d) battery in charge.
6. Plethysmography curves and tendency lines visualization capabilities for
monitored parameters.
7. At least the following audio alarms:
a) high frequency.
b) low frequency.
c) low saturation.
8. Components
 Case is to be hard and splash proof.
 Display must allow easy viewing in all ambient light levels.
 Supplied in protective case for clean storage and safe transport.
 Handlebar or facilities for easy transportation.

9. UTILITY REQUIREMENTS
 Electrical DC Charger electrical source requirements:
 Voltage input: _220v; Frequency 60hz:
 Protections against over-voltage and over-current line
conditions.
 Battery charger
 Battery to allow at least eight hours’ continuous operation.

10. ACCESSORIES, CONSUMABLES, SPARE PARTS, OTHER COMPONENTS

 Accessories Battery charger, Batteries
 Oximeter cable with a length of at least 1.2 m.
 1 adult patient reusable oximeter sensors.
 1 pediatric patient reusable oximeter sensor.
 1 neonatal patient reusable oximeter sensor.

11. TRAINING, INSTALLATION

 Training of users/s Training of users in operation and basic
maintenance shall be provided.
 Advanced maintenance tasks required shall be documented

 Users care the case is to be cleanable with alcohol or

chlorine wipes.
12. WARRANTY AND MAINTENANCE
 Warranty two year
13. DOCUMENTATION
 Documentation requirements User and maintenance manuals to be
supplied in English language.
 Certificate of calibration and inspection to be provided.

14. SAFETY AND STANDARDS

 Regulatory Approval / Certification Must be FDA, CE or UL approved
product.
2. Technical specification for otoscope
1. Generic name Otoscope
2. Quantity each 03
3. Detailed requirements
o At least 2.5 V Xenon or Halogen light source.
o Fiber optic direct transmission of the light.
o Swiveling viewing with at least 3x magnification.
o Specula compatible/fitting with the otoscope head provided.
o Insufflation port for pneumatic test of tympanic mobility.
o Soft ball and tube for pneumatic tests.
o Hard case for keeping at least otoscope head, handle and
specula.
4. Components
 On/off switch to be robust and easy to use
 External material to be non-ferrous.
 Pivoting head
 Interchangeable specula
5. Mobility, portability
 Handheld unit, single piece when in use.
 Supplied in protective, re closable container.
6. UTILITY REQUIREMENTS
 Internal batteries, rechargeable preferred.
 Battery charger with power input to be 220v 50HZ fitted with compatible
mains plug.
 Battery compartment to be sealed against liquid ingress, yet easily opened.
o Rechargeable batteries with at least the following characteristics:
 At least n. 3 battery chargers (integrated or external)
compatible with both 2.5 V and 3.5 V batteries or handles
provided.
 Led display indicating the charging status.
 Charger electrical source requirements: Voltage: 220v__.
 Charger electrical source with line connection plug type.
 Table or wall power source holder.
 Protections against over-voltage and over-current line conditions.
 Compliance with electrical standards and regulations
7. ACCESSORIES
 Accessories Set of plastic specula, varying diameters between 2.0 and
5.0 mm.
 Two spare bulbs
 At least n. 10 reusable (autoclavable) otoscope specula for each one of
the following measures: 2, 3 and 5 m
8. TRAINING, INSTALLATION AND UTILISATION
 Training of user/s Training of users in operation and basic maintenance
shall be provided.
9. WARRANTY
 Warranty in two years
10. DOCUMENTATION
  Documentation requirements Advanced maintenance tasks required shall be
documented.
 User, technical and maintenance manuals to be supplied in English language.

11. SAFETY AND STANDARDS

 International standards
 IEC 60601-1-2:2007 Medical electrical equipment - Part 1-2: General
requirements for basic safety and essential performance - Collateral standard:
Electromagnetic compatibility - Requirements and tests
 IEC 60601-2-18 Ed. 3.0:2009 (b) Medical electrical equipment - Part 2-18:
Requirements for the basic safety and essential performance of endoscopic
equipment

3. Technical specification for wheelchair

1. Generic name : wheelchair
2. Quantity: 20 each
3. feature
 Width 20-inch Seat Width
 Weight Capacity 250 lbs/115 kg
 Seat Depth 16"
 Seat Height 18.5"
 Back Height 17"
 Overall, Height 36"
 Overall Open Width 24.5"
 Overall Folded Width 11"
 Front Caster Size 8"
 Rear Wheel Size 24"
 Product Weight (without Riggings) 36lbs/17kg
4. Warranty one year
5. Documentation
 Installation manual in English
6. Training and installation
The company must provide user training.
7. Safety and regulation
Provide appropriate certificate FDA and FMHACA
4. Technical specification for I.V. Stands
1. Generic name I.V stand
2. Quantity 300 each
3. Feature
 Two-piece telescoping 1˝ (25mm)-diameter tubular 16-gauge type 304
stainless steel pole Corrosion Resistance, Rustproof.
 20˝ (51mm)-diameter, 17-lb. (7.7 kg), five-leg black epoxy coated
height-weight base.
 3˝ (76mm) premium swivel casters with rubber wheel— two with
brake.
 Knob-operated height adjustment from 68˝ to 99˝ (1727 to 2515mm).
 Four-hook top.
 Holds up to 20 lbs. (9.0 kg) of I.V. fluid.
4. Easy-to-clean surfaces.
5. Patient handle & accessory tray
6. Two-cylinder holder
7. Electrical strip
8. Wire basket
9. Warranty one year
10. Documentation
 Installation manual in English
11. Safety and regulation
Appropriate certification from FDA and FMHACA

5. Technical specification for patient record trolley

1. generic name Trolley - Patient Record
2. Quantity Each 40
3. feature
 Steel tube frame. Construction fully welded. Finish: epoxy
 Upper tray, back and side panels in beige laminate
  Designed to hold 2 rows of filing pockets: 32 compartments (16 by
level).
 Resin partitions - Handles
 Wheel bumpers
 Rolling shutter with key lock
 Swivel ball-bearing castors Ø 125 mm
4. Warranty one year
5. Documentation
Installation and user manual
6. Training and installation
 Installation manuals provide in English.
7. Safety and regulation
 Appropriate certification from FDA and FMHACA
6. Technical specification for stethoscope /adult/infant
1. Generic name: Stethoscope
2. Quantity: Each 70
3. Detailed requirements
 Bi-aural unit.
 Double stent chest piece.
 Plain spring non-folding frame.
 Plastic ear tips.
 Vinyl stethoscope tubing.
 Combined bell and diaphragm Sprague type.
4. Components
 Two earpieces
 sprung to stay fixed in ears.
 Dual head: Cup/bell for low frequency sounds, membrane for skin
contact pickup
 Cup or membrane use selected by secure.
 easy to use mechanism.
 Raw Materials Head and earpiece constructed of non-ferrous material.
 Earpieces to have shaped, cushioned ends.
 Tubes to be synthetic material.
 Supplied in protective, re closable container.
5. ACCESSORIES, CONSUMABLES, SPARE PARTS, OTHER
COMPONENTS
 Accessories Spare set of earpieces
 Two spare membranes
 flexible ear tips, tubing, ear tube, membranes or diaphragms.
6. TRAINING, INSTALLATION AND UTILISATION
 Pre-installation requirements Supplier to perform installation, safety and
operation checks before handover.
 Training of users Training of users in operation and basic maintenance shall
be provided.
7. User care
 Cleaning All parts cleanable with alcohol or chlorine wipes, and warm
soapy water
8. WARRANTY AND MAINTENANCE
 Warranty one year
9. DOCUMENTATION
 Documentation requirements
 User, technical and maintenance manuals to be supplied in english language.
 List to be provided of equipment and procedures required for local calibration
and routine maintenance.
 List to be provided of important spares and accessories, with their part
numbers and cost. Certificate of calibration and inspection to be provided.
10. SAFETY AND STANDARDS
 Must provide appropriate certification from FDA and FMHACA
7. Technical specification Sphygmomanometer (manual B.P apparatus)
1. Generic name Sphygmomanometer
2. Quantity each 60
3. Detailed requirements
- Cuff arm fixing method to allow ease of use, ease of cleaning and low
attraction of dirt.
- Washable size adjustable cuff (one size fits all).
- Pressure gauge to allow reading of pressure to 2mmHg accuracy.
- Maximum pressure to be at least 300mmHg.
- Gauge body to allow recalibration of readings, yet in normal operation
be sealed and secure.
- Displayed parameters mmHg
- Components Rubber tubes to be detachable from other parts,
allowing periodic cutting of decayed ends.
- Gauge body to include clip for mounting on cuff.
- Tube length to be greater than 30cm.
- Cuff surround to be removable and washable.
- To be supplied in protective, re closable container
15. TRAINING, INSTALLATION AND UTILISATION
 Training of user/s Training of users in operation and basic maintenance shall
be provided.
16. WARRANTY AND MAINTENANCE
 Warranty two year
17. DOCUMENTATION
 User, technical and maintenance manuals to be supplied in English language.
 Certificate of calibration and inspection to be provided.
 Contact details of manufacturer, supplier and local service agent to be
provided.
18. SAFETY AND STANDARDS
 Regulatory Approval / Certification Should be FDA, CE or UL approved
product.

8. Specification for delivery couch

1. Generic name delivery couch
2. Quantity 6 each
3. feature
 Overall Size 1800*800*750mm
 Frame Dia 35mm
 Mattress 50 mm (h)
 Bowl or tray, capacity 3 liters.
 Loading capacity 150kgs
 Bed with epoxy painted frame.
  Three sections with independent controls.
 Mounted on 4 adjustable rubber feet.
 Removable padded mattresses with removable, washable, fire-retardant cover
by with zip density of mattresses 30 kg/m3
 Back section adjustable by ratchet
 Pelvic section adjustable by infinitely adjustable crank
 Fitted with patient hand grips.
 Knee crutches holder welded to the frame.
 Knee crutches and leg holders adjustable in height and width
 Fitted with removable liquid tray.
4. Documentation
 User manual and installation manual must be provided.
 All necessary installation must be provided by company
5. Warranty
 Warranty at least two years
6. Safety and regulatory
 Must provide appropriate certification from FDA and FMHACA
9. Gynecology couch examination specifications
1. Generic name delivery couch
2. Quantity 8 each
3. Feature
 Made of epoxy coated steel
 Two sections: Body section: mounted on four rubber feet.
 Leg section: mounted on four 100mm diam. castors two of which with
brake.
 Folding section under body by tracks with nylon roller.
 Foam mattress density 30 kg/m3, height 10cm
 Padded mattress with zip removable from bed
 Carrying capacity 150 kg
 Complete with leg holders
4. Knock down construction.
 Body section 1000*900*750mm
 Leg section 900*850*750mm
 Swivel castors Dia 120mm
 Thickness of matters 100 mm (H)
 Loading capacity 150kg
10. Crash cart technical Specifications:
1. Generic name crash cart
2. Quantity each 8
 12.5cm swivel media castors, two are breaking
 Corner buffers
 Oxygen Cylinder Holder provision
 I.V. Rod provision
 Cardiac massage board & 3 laminated shelves
 Overall approx. size: 940mmL x 490mmW x 1535mmH
 Six removable bins
 Two Polystyrene storage units with three drawers each.
3. Documentation
Installation and user manual
4. Training and installation
Training for user
5. Safety and regulation
Approved certification from local or international organization

11. Technical specification Fetal Doppler ultrasound

1. Generic name fetal doppler ultrasound
2. Quantity each 02
3. Feature

 7” TFT digital display screen

 Oscilloscope Waveform display of twins heart rate (FHR), Uterine

contraction pressure (TOCO) value and automatic detection of fetal

movement.

 Curve display and Big front display also available

 4.8 V 2200 mAh Li-ion Battery rechargeable with 4 hours of continuous

working

 Auto power failure protections for continual monitoring

 112 mm printer with real time printing and storage printing available

 Dimensions: 296 x 312 x 92 mm

 Power Supply: AC: 100-240V, 50/60 Hz±1 Hz, 40VA

 Ultrasound working frequency: 2Mhz, 2.5Mhz

4. Documentation
  Must be provide all necessary document. User manual in English

5. Training and installation

 Company must provide user and technical training

6. Warranty

 Warranty at least two years

7. Safety and regulation

12. Technical specification Glucometer with strip

1. Generic name: glucometer
2. Quantity: each 35
3. General feature:
 Weight 0.2 lbs. (75 g)
 Dimensions 3.6 in x 2.3 in x 0.9 in (91 mm x 58 mm x 23 mm)
 Data Storage 400 glucose measurements or QC tests
 Measurement Range and Units
 U.S. 10-900 mg/dL
 Outside U.S. 1-50 mmol/L
 Blood Glucose Measurement
 Sample Volume Required 1.2uL
 Time to Glucose Results 6 seconds
 Connectivity
 Data Transfer Strip Port Connection to USB
 Data Program Nova Microsoft-Excel based data transfer Software.
 Battery Information
 Type 3V Li Button Battery
 Features Replaceable
 Life Minimum 600 tests before battery requires replacement.
 Interferences Corrected for by StatStrip Xpress Meter
 Hematocrit, Ascorbic Acid, Acetaminophen, Uric Acid, Maltose, Galactose,
and Oxygen
 Additional Features
• LCD black/white display
• Large numeric display (30 mm)
• Traditional QC with target values assigned to QC materials
• Units of measure based on meter ordered (mg/dl or mmol/L models)
• Auto shut off of meter when not in use
• Automatic sample detection and analysis start
• Automatic sample counter with date/time stamp for data tracking
 Test Strips
 Test Strips available in cases of 1800 or boxes of 100.
 QC Test Solutions
 QC Test Solutions of low, medium, high, and very high concentration are
available to confirm calibration of the Stat Strip Xpress meter.
4. Documentation
  Must be provided with all necessary document. User manual in English

5. Training and installation

 The company must provide user and technical training.

6. Warranty

 Warranty at least two years

7. Safety and regulation
 Regulatory Approval / Certification Must be FDA, CE or UL approved
product.

13. Technical specification Light-Operating, Mobile

1. Generic name: light oprating
2. Quantity each 10
3. General feature
 The light use 48LEDS (main bulb) +144LEDS (auxiliary bulb) LED
light source (light cup is one main and three auxiliary bulb structure),
divided into multiple independent illuminant group; Each light uses dual
CPU control, every group of the LED light source controlled by special
circuit chip, any group failure will not affect the normal use.
 Light head diameter: Ø670 mm
 Color temperature: 3000 K - 5000 K
 Color rendering index, Ra CRI: 96%
 Illuminance can be adjusted from: % 1 – 100.
 Light field diameter d50: 13 – 28 cm / 5.1” – 11”
 Number of LED modules: 60
 Lifetime of LED: >60.000 h
 Degree of turbulence (standard value 37.5 % max.): 29%
 Depth of the volume of light L1 + L2 at 20 %: 130 cm / 51.2”
 Depth of the volume of light L1 + L2 at 60 %: 76 cm / 30”
 Irradiance at nominal illuminance: 510W/m2
4. Documentation

 Must be provided with all necessary document. User manual in English

5. Training and installation

 The company must provide user and technical training.

6. Warranty

 Warranty at least two years

7. Safety and regulation
14. Technical Specification: Volumetric Infusion pump
1. Generic name: infusion pump
2. Quantity
3. General feature
 Gross weight ＜4 kg
 Power supply AC220 -240V.50/60HZ (should operate on single phase
power supply in Ethiopia)
 Fuse 2 pcs of 220V0.5A, 2 pcs of 1.5A
 Infusion rate range 1- 1000 ml/h
 Infusion increment 1ml/h
 Injection accuracy h ±3%(after being well adjusted, up to ±2%)
 KVO rate
 Bolus rate 1ml/h 600ml/h 1~9999ml
 Accumulated volume
 Preset range 1~9999ml
 Alarm function AIR, OVER, OCCL., no AC power supply, low
battery, serious low battery, error 1/2/3/4 1
 Occlusion value 39.2kPa-137.2kPa
 Battery Rechargeable lithium polymer battery with 2 hrs backup
 EMC Meet the requirements of IEC60601-1-2(2007 version)
 Electrical safety Meet the requirements of EN60601-
1:1990+A1:1993+A2:1995
 Operation condition Environment temperature: 5℃ ～ +40℃, air
pressure (86～106) kPa, relative humidity≦80%
 Storage condition Environment temperature: -20℃ ～ +50℃, air
pressure (50 ～ 106) kPa, relative humidity≦95% ①infusion rate
②infusion preset volume ③accumulated infusion volume.
 panel instructions ④battery capacity ⑤battery charging indication
⑥AC power supply connection indication ⑦over ⑧OCCL. ALARM
⑨air ⑩Bed No.,
8. Documentation
User manuals provide with English language.
9. Training and installation
User and technical training for clinical staff and biomedical
10. Safety and regulation
Must provide appropriate certification from FDA and international
organization.

15. Technical specification for sphygmomanometer-Digital, Adult/Ped. /Infant

1. Generic name electronic blood pressure monitor
2. Quantity 73
3. Overview of functional requirements
 The main unit controls and displays numerical data for BP. It also
includes appropriate attached cuffs (probes, and sensors, depending on
their configuration) that allow sequential, periodic and/or simultaneous
measurements.
 Detailed requirements Measurement ranges: systolic (mm Hg), 60–
250, 290 preferred for adults, 30–160 for children and 20–120 for
 neonates. Diastolic (mm Hg), 30–180 adults, 10–150 pediatrics, 10100
neonates.
 Mean arterial pressure (mm Hg), 30–250 adults, 30–160 children, 30–
110 neonates. Pulse (beats per min), 30–150 adults and children, 30–
180 neonates.
 Inflation pressure (mm Hg) 150–260 adults, 85–140 neonates;
adjustable or automatically set preferred. Auto deflate pressure (mm
Hg), 300 adults, 150 neonates.
 Measurement interval, min: User selectable: ≥ 5 choices. Cuff sizes:
neonatal, pediatric, adult, large adult, thigh. Measurement time (s) ≤ 60,
user selectable. Automatic 0 required.
 Display may include tabular and/or graphic trends (user preference).
Equipment alarms required: cuff leak, cuff disconnect, failure to take
successful reading, low-battery notice.
 Equipment alarms preferred: hose leak, inflation or deflation error.
Sphygmomanometer should automatically deflate if the cuff pressure
reaches 300 mm Hg for an adult and 150 mm Hg for a neonate.
 Displayed parameters the unit should display the following numerical
values: systolic pressure, diastolic pressure, pulse rate and mean arterial
pressure.
 unit should alert the operator, either visually or audibly.
 User adjustable settings Inflation pressure should be adjustable or
automatically set according to a previous or current pressure reading or
individual requirements.
 Time between automatic BP measurement cycles should be selectable
from at least five values over a range of 1 to 60 min. Set alarm volume
and limits within the specified measurement ranges. Physical and
chemical characteristics
4. Components Rubber tubes to be detachable from other parts, allowing periodic
cutting of decayed ends. Gauge body to include clip for mounting on cuff. Tube
length to be > 30 cm. Different cuff sizes available (small or neonate, medium
or pediatric, large or adult and extra-large or large adult). Cuff material to be
removable and washable.
5. Utility requirements Electricity, water and/or gas (if relevant) AC: 120/240,
50/60 Hz DC: Rechargeable battery (for at least 1 h of operation, single-use or
rechargeable) Accessories, consumables, spare parts, other components
6. Accessories Mobile stand 26 Sterilization process for accessories (if relevant)
Not applicable 27 Consumables and reagents (if relevant) Single-use cuffs in
the following sizes: neonatal (10–15 cm), pediatric (14–22 cm), adult (25–36
cm), large adult (34–43 cm), thigh (40–55 cm). The sizes of the cuffs depend
on the manufacturer but should not deviate by ± 5 cm from the stated sizes.
Batteries 28 Spare parts (if relevant) Rubber tube (length > 30 cm), reusable
cuffs in the following sizes: neonatal (10–15 cm), pediatric (14–22 cm), adult
(25–36 cm), large adult (34–43 cm), thigh (40–55 cm). The sizes of the cuffs
depend on the manufacturer but should not deviate by ± 5 cm from the stated
sizes. Tubing, valve
7. Training of users All users (physicians nurses, other medical staff) shall have
initial training in operation. Biomedical or clinical engineer or technician,
medical staff, shall have initial training in operation and basic maintenance by
manufacturer, and subsequently if necessary.
 8. Warranty 2 years
9. Safety and standards Regulatory approval or certification Proof of regulatory
compliance (e.g., registration, clearance, approval) must be provided as
appropriate per the product’s risk classification, by regulatory agency (e.g. by a
founding member of IMDRF-EU, USA, Canada, Australia, Japan

16. Steam sterilizer technical specification

1. Generic name steam sterilizer
2. Quantity each 2
3. General feature
 Capacity:
About 175 liters per load
 Working pressure:
200 kPa or higher (sterilizing mode)
 Working temperature:
134°C (sterilizing mode)
 Footprint:
Compact footprint: 1.1 m x 1.5 m x 2 m high
 Pressure vessel standard
Complies with ASME Boiler and Pressure Vessel Code
Section VIII and RSA/CI-OSHA-81-2010 A2011 – certificate to
be provided.
 Outside steam jacket
Yes
 Vacuum system and vacuum requirements
Steam ejector system capable of achieving -60 kPa; meets.
section 8.2.2 of EN 285:2006+A2:2009 (i.e., uniform color
change throughout a Bowie-Dick indicator when tested on the
empty autoclave)
 Required sequential modes of operation.
Steam mode 1 up to 180 kPa
Vacuum mode 1 to -50 kPa
Steam mode 2 up to 180 kPa
Vacuum mode 2 up to – 50 kPa
Sterilizing mode for 15 minutes
Drying mode for 10 minutes
Door release mode
 Controls
The autoclave shall be operated by manual controls.
(Mechanical wheel and cam system) to permit manual.
operation following the required sequential modes of
operation specified above.
 Safety feature – redundant overpressure
features
Overpressure safety relief valve and pressure limiting control.
to keep the pressure below the maximum allowable pressure
 Safety feature – door interlock
Door interlock system to prevent opening door while vessel is
under pressure, safety feature shall also prevent start-up if the
 door is not properly closed.
 Safety feature – emergency shut-off.
Shut-off as part of the manual control.
 Safety feature – protection from hot
surfaces
External insulation to prevent workers from coming in contact.
with hot surfaces (exceeding 50°C)
 Safety feature – accidental vacuum
breaker
Vacuum breaker valve to introduce air when breaking the
vacuum
 Materials of construction:
Main shell – 304L stainless steel; jacket cells – A240 type
304L stainless steel

o Door:
Quick opening sliding door with expanding gasket
Pressure gauge readable by normal vision from a distance of
(1.00 ± 0.15) m
 Other indicator displays:
Light indicating power on; other displays as needed
Indicator for temperature
± 1% accuracy or better over the scale range 50°C to 150°C
Indicator for pressure
± 1.6% or better over the scale range -1 bar to 3 bar
Recording:
Recording of temperature using a graph or printout; printed
records should be readable for 3 years.
 Decontamination of air:
Air removed during the vacuum cycle must be
decontaminated by mixing with steam to prevent release of
pathogens
 Loading and unloading system:
Waste is collected inside a horizontal barrel (carriage)
mounted on a trolley (see below); the barrel is locked to the
trolley during transport and can be unlocked and pushed into
the autoclave chamber for treatment
 Markings:
Markings for safety shall comply with ASME BPV Code
Section VIII
Required auxiliary equipment:
Steam generator
24 kW steam generator (boiler) mounted under the autoclave.
chamber.
4. Electrical:
380-400 VAC, 3-phase, 50-Hz
Display indicators:
5. Safety and standard
 Electrical safety:
Meets the requirements of IEC 61010-2-040, UL 61010A-2-
 041, or equivalent electrical safety standard
 FDA and European standard certification must provide.
 documentation
 Operating and service manual in English
 warranty
One (1) year warranty on parts and service after
commissioning and acceptance
On-site training is provided to operators.

17 technical specification Monitor – Patient

1. Generic name
2. Quantity 24 each
3. General feature
A. Display Monitor
a) At least 12 inches size
b) Color TFT touch screen
c) Capable of displaying 4 to 6 waveforms
B. ECG/Cardiac Monitoring
a) ECG waveform display (at least 3 waveforms; Lead I, lead II, Lead III) and
with corresponding beep sound on each QRS waveform.
b) Heart rate display
c) With Arrhythmia Analysis, ST Calculation and Pace Analysis
d) Lead selection switch
e) Sensitivity switch: 2.5 to 2.0 mm/mv
f) Filter switch for interference from: Mains power frequency Low and high pass
signal
g) Common Mode Rejection (CMR): more than +100dB
h) ECG signal measurement range: -2mV to +2mV
i) Frequency range: At least 0.67 to 150Hz or wider range
j) Input impedance: 2.5 MΩ at 10Hz k) Frequency response: -3db at 0.5Hz to
100Hz l) Automatic internal data storing for at least 40 ECG records
m) ECG leads connector for at least 3-lead patient cable (protection from
interference) n) Patient cable with at least 3 leads and with electrical screening
o) ECG recorder/printer capable of printing at least 4 waveforms simultaneously,
Arrhythmia Analysis, ST Calculation and Pace Analysis and heart rate, etc.
C. Pulse Oximeter
a) Hinge finger probe or rubber finger probe and ear sensors for adult, pediatric
and infant use. The connection of the probes to the main unit must have locking
mechanism.
b) Oxygen saturation (SpO₂): 70 up to 99% with minimun graduation of 1%.
c) Pulse rate in beats per minute (bpm). Pulse rate range at least 30 to 240 bpm,
with minimum graduation of 1 bpm.
d) Pulse waveform or indicator that illustrates the strength of pulse being
detected.
e) SpO₂ limit alarm activation settings
f) Pulse rate limit alarm activation settings
g) Alarm sound level adjustment and alaram override and temporary silence
control. a. Accuracy of SpO₂ measurement: ±3%
h) Accuracy of pulse rate measurement: ±5 bpm
 D. Temperature Measurement
a) Digital Thermometer
b) Body temperature measured at degrees Celsius with measurement range of
32-43⁰C c) Measurement accuracy: +/- 0.1⁰C between 35⁰C to 41⁰C
E. Non-Invasive Blood Measure Monitor (oscillometer method)
a) Inflatable rubber cuff surrounded by durable and flexible cover with
Velcro strips b) Rubber tubes eight at least 30cm in length
c) Systolic and diastolic blood pressure measurement with a maximum
pressure reading of 300mmHg
d) Reading accuracy: ±5mmHg or better
e) Measures blood pressure at least every 10 minutes
F. Respiratory Monitoring
a) Thoracic impedance measurements via ECG leads
b) Breaths per minute with measurement range of 0-120 BPM
c) Respiratory waveform display
d) Measurement accuracy: ±3 BPM or better
G. Safety Features
a) Protection against defibrillation and electrosurgical equipment
b) Equipment compatible with patients with pacemakers
c) Degree of protection against electrical shock: Type CF
d) Alarms (the equipment must have an alarm setting switch and sound
adjustment switch)
i. Arrhythmia
ii. Ventricular fibrillation
iii. Tachycardia
4. documentation
 user manual prepared by English language.
5. Warranty two years
6. training and installation
 must provide training for clinical staff and biomedical staff.
7. safety and regulation
must provide FDA certification.

18 Patient bed side table with medication cabinet

1. Generic name Patient bed side table
2. Quantity 317
3. General feature
ITEM PARAMETERS
Minimum height 85cm
Expansion length 102cm
Folding length 59cm
Sideboard size 45*31.5cm
Sideboard height 77-102cm
Drawer size 40*33*8cm
Small cabinet size 44*36.5*24cm
Hollow inter-layer 44*36.5*25cm
Table size 51*40cm
4. Documentation
User and installation manual must be provided.
5. warranty one year
6. Training and installation
 User training must be provided.
7. Safety and standard
Approval certification must be provided.
19.Specification for Stethoscope – Neonatal
20. Crash Chart (5 Locked Emergency medication cabinate) ??????