Patient Monitor

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Patient Monitor

Purchaser Specification
S.N. Patient Monitor
Manufacturer
Brand
Type / Model
Country of Origin
1. Description of Function
1.1 Advance monitoring vital signs of all patient categories, at bedside, transportation
applicable for Pediatric and neonatal application
2. Operational Requirements
2.1 It shall operate on AC power supply as well as built-in battery.
3. System Configuration
3.1 Should have ECG, SpO2, NIBP, Respiration and Temperature
4 Technical Specifications
4.1 Advanced High end ICU Monitor for Pediatric and neonatal application
4.2 Should have 12” or more high resolution screen
4.3 Should have facility to display ECG, SpO2, NIBP, Respiration and temperature
simultaneously
4.4 Should display at least 8 waveforms of selected parameters simultaneously
4.5 Monitor should work on Fan-less technology
4.6 Measurements range:
4.6. HR approximately 15 to 270bpm
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4.6. NIBP approximately 20 to 270mmHg
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4.6. SpO2 approximately 0 to 100%
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4.6. NIBP oscillometric step deflation, manual/automatic, initial inflation pressure user
4 selectable
4.6. Must have patient specific alarm limit display on main screen.
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4.6. Shall have defibrillator sync and protection during defibrillation.
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4.6. Display shall have facility to report system errors, leads and sensors failure and built-in
7 battery status.
4.6. Autonomy of built-in Lithium ion rechargeable battery approximately 2 hours,
7 automatic recharge when connected to mains.
4.6. Automatic switch to batteries in case of power failure.
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5 Accessories, spares and consumables
5.1 Accessories:
Should be supplied with standard accessories.
 3 lead ecg electrode cable -2 pc
 Neonate Spo2 probe-2 each
 Neonate NIBP Cuff- 2 each
 Temperature probe: Skin and Rectal- 1 each
5.2 All standard accessories, consumables and parts required to operate the equipment,
including all standard tools and cleaning and lubrication materials, to be included in the
offer.
6.0 Operating Environment
6.1 The system offered shall be designed to operate normally under the conditions of the
purchaser's country. The conditions include Power Supply, Climate, Temperature,
Humidity, etc.
6.2 Power supply: 220 - 240 VAC, 50Hz fitted with appropriate plug.
7 Standards and Safety Requirements
7.1 Must submit ISO 9001 or ISO 13485:2003/AC:2007 for medical devices AND
7.2 CE (93/42 EEC Directives) and USFDA approved product certificate. Self declared CE
certificate will no be accepted.
7.3 Shall meet IEC-60601-1-2:2001 General Requirements of Safety for Electromagnetic
Compatibility. Document evidence shall be submitted for evaluation
8.0 User Training
8.1 The Supplier shall conduct user training for this equipment to enable operators to use the
equipment properly. The training shall include the use of all operational functions of the
equipment, as well as routine checks and maintenance expected by users.
9.0 Warranty
9.1 Warranty for 2 year after acceptance.
10.0 Maintenance Service During Warranty Period
10.1 During the warranty period supplier must ensure corrective/ breakdown maintenance
whenever required.
11.0 Installation and Commissioning
11.1 The bidder must arrange for the equipment to be installed and commissioned by
certified or qualified personnel; any prerequisites for installation to be communicated to
the purchaser in advance, in detail.
12 Documentation
12.1 User (Operating) manual in English.
12.2 Service (Technical / Maintenance) manual in English.

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