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NOTE
Important!
Read the operating instructions.
Classification:
• Internally powered equipment
• BF type applied part
• IPX0
• Not suitable for use in presence of flammable anaesthetic mixture with air or with oxygen or
nitrous oxide
• Continuous operation with short-time loading
This Blood Pressure Monitor complies with the EC Directives and bears the CE Mark "CE
0197".
The quality of the device has been verified and is in line with the provisions of the EC council
directive 93/42/EEC (EN IEC60601-1 — General requirements for safety, EN IEC 60601-1-
2:2001 — Electromagnetic compatibility-Requirements and tests) dated 14 June 1993
concerning medical devices and the EN performance standards as follow:
EN 1060-1:
Non-invasive sphygmomanometers - General requirements
EN 1060-3:
Non-invasive sphygmomanometers - Supplementary requirements for electromechanical blood
pressure measuring systems.
EN 1060-4:
Non-invasive sphygmomanometers - Test procedures to determine the overall system accuracy
of automated non-invasive sphygmomanometers.
GB
GB
BM101 10/16/06 12:15 PM Page 24