User's Manual

Patient Monitor User Manual Product Specification
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A Product Specification
A.1 Classification
Anti-electroshock type Class I equipment and internal powered equipment
Anti-electroshock degree ECG (RESP), TEMP, IBP, C.O., Quick Temp CF
SpO
2
, NIBP, CO
2
, AG BF
Ingress Protection IPX1 (No protection against ingress of water if configured
with Quick TEMP module)
Disinfection/sterilization method Refer to Chapter Care and Cleaning for details.
Working system Continuous operation equipment
Compliant with Standards IEC 60601-1: 1988+A1: 1991+A2: 1995; EN 60601-1:
1990+A1: 1993+A2: 1995; IEC 60601-1-2: 2001+A1:
2004; EN 60601-1-2: 2001+A1: 2006; ISO 9919, ISO
21647, IEC/EN 60601-2-27, IEC/EN 60601-2-30, IEC/EN
60601-2-34, IEC/EN 60601-2-49, ANSI/AAMI SP10,
AAMI/ANSI EC13, EN12470-4 EN1060-1 EN1060-3,
EN1060-4, IEC/EN 60601-2-25*, IEC/EN 60601-2-51*
(Symbol * means this standard only applicable to iM80)
A.2 Physical Specifications
A.2.1 Size and Weight
Product Size Weight (standard
configuration, without
battery)
iM50 261 mm (L) × 198 mm (W) × 215 mm (H) <3.6 kg
iM60 303mm(L) × 161mm(W) × 254mm(H) <4.5 kg
iM70 328mm(L) × 158mm(W) × 285mm(H) <5.5 kg
iM80 370 mm (L) × 175 mm (W)× 320 mm (H) <7 kg
A.2.2 Environment Specification
The monitor may not meet the performance specifications given here if stored or used outside the
specified temperature and humidity ranges.
When the monitor and related products have differing environmental specifications, the effective
range for the combined products is that range which is common to the specifications for all
products.