Welch Allyn Medical Diagnostic Equipment Medical Alarms 8.1x Manual Do Utilizador

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Chapter 1   General information
Welch Allyn  Acuity Central Monitoring System
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
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.