Welch-allyn Acuity and Mobile Acuity LT Central Monitoring Sys Manual de usuario descargar pdf (Pagina 11)

Directions for use Chapter 1 General information 7

Acuity System compliance with safety standards

The CE Mark and Notified Body Registration Number signify that the product meets all essential

requirements of European Medical Device Directive 93/42/EEC.

Table 1. Acuity System compliance with safety standards

Acuity System component(s) Product category Organization and

standard

Propaq Encore, Propaq CS, Propaq LT, Welch Allyn

1500 Patient Monitor and Micropaq monitors

Wireless Micropaq, Propaq LT and Propaq CS

monitors

Medical Equipment EN 60601-1:1990

A1:1992, A2:1995

IEEE 802.11, Wireless

LAN Medium Access

Control (MAC) and

Physical Layer (PHY)

Specifications

IEEE 802.11a, 802.11e,

802.11h, 802.1X, 5 GHz

All components operating together as a system Electromagnetic compatibility for

Medical Equipment

IEC 60601-1-2:2007

All components operating together as a system Medical Systems IEC 60601-1-1:2000

All information systems components Information Technology Equipment EN 60950:1994

Acuity System cordless receiver cabinet Electromagnetic compatibility FCC Class A

a. When the equipment is operated in a commercial environment, Class A limits provide reasonable protection against

harmful interference. The equipment generates, uses and can radiate radio frequency energy; if it is not used in

accordance with this reference guide, or if it is modified from original installation, it might cause harmful interference

to radio communications. Operation of this equipment in a residential area is likely to cause harmful interference, in

which case the user is required to correct the interference at his own expense.

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Welch-allyn Acuity and Mobile Acuity LT Central Monitoring Sys Manual de usuario Pagina 11