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11
English
Subject to change without notice.
This device conforms to the following standards:
EN 60601-1:2006/A1:2013 - General requirements for basic safety and essential performance.
EN 60601-1-2:2015 - Medical Electrical Equipment - Electromagnetic compatibility - Requirements and tests.
EN 60601-1-11:2010 - Medical Electrical Equipment - Requirements for medical electrical equipment and medical electrical
systems used in the home healthcare environment.
EN 1060-3:1997 + A2:2009 - Non-invasive sphygmomanometers - Supplementary requirements for electromechanical blood
pressure measuring systems.
EN 1060-4:2004 - Non-invasive sphygmomanometers - Test procedures to determine the overall system accuracy of
automated non-invasive sphygmomanometers.
This product conforms to the provisions of the EC Directive 93/42/EEC (Medical Device Directive and
superseding regulations).
This product carries the CE mark and is manufactured in conformity with the RoHS Directive 2011/65/EU.
MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding EMC.
For a detailed description of EMC requirements please contact an authorised local Service Centre (see guarantee) or visit
www.hot-europe.com/support.
Portable and mobile RF communications equipment can aect medical electrical equipment.
This product contains batteries and recyclable electronic waste. To protect the environment, do not dispose
of it in household waste, but take it to an appropriate local collection centre provided in your country.
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