Patient Monitor User Manual Product Specification
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A Product Specification
A.1 Classification
Class I equipment and internal powered equipment
(RESP), TEMP, IBP, C.O., Quick Temp CF
IPX1 (No protection against ingress of water if configured
Disinfection/sterilization method
Refer to Chapter Care and Cleaning for details.
Continuous operation equipment
IEC 60601-1:1988+A1+A2, EN 60601-1:1990+A1+A2,
IEC/EN 60601-1-2:2001+A1, ISO 9919, ISO 21647,
IEC/EN 60601-2-27, IEC/EN 60601-2-
60601-2-34, IEC/EN 60601-2-49, ANSI/AAMI SP10,
IEC/EN 60601-2-25, AAMI/ANSI EC13, EN12470-
EN1060-1 EN1060-3, EN1060-4
A.2 Physical Specifications
A.2.1 Size and Weight
370 mm (L) × 175 mm (W)× 320 mm (H)
260 mm (L) × 140 mm (W)× 205 mm (H)
A.3 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.
25% ~ 80% (non-condensing)
25% ~ 93% (non-condensing)