visomat comfort III Mode D'emploi page 50

G
Explanation of symbols
This blood pressure monitor conforms to Council
Directive 93/42/EEC of 14 June 1993 on Medical De-
vices and bears the mark CE 0123 (TÜV Süd Product
Service). Devices with CE marks are quality-con-
trolled in accordance with this Directive and provide a
higher level of accuracy than previous calibration.
Degree of protection against electric shock:
TYP BF
Observe Instructions for Use
Batteries and appliances must not be dis-
posed of with domestic waste but should be
handed in at the appropriate collection and
disposal points.
The requirements of the following standards are met:
GB-50
All manuals and user guides at all-guides.com
• EN 1060-1: 1995
Non-invasive sphygmomanometers
Part 1: General Requirements
• EN 1060-3: 1997
Non-invasive sphygmomanometers
Part 3: Additional Requirements on electro-
mechanical blood-pressure measuring devices
• EN 1060-4: 2004
Non-invasive sphygmomanometers
Part 4: Test procedure for establishing
accuracy
• ESH (European Society of Hypertension)
The monitor satisfies the clinical testing
requirements of the «International Protocol for
validation of blood pressure measuring devices in
adults, 2002".
Appendix