Braun iCheck 7 Manual De Instrucciones página 13

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.
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 affect medical electrical equipment.
Hereby, Kaz Europe Sàrl, declares that the radio equipment type BPW4500 is in compliance with Directive 2014/53/EU.
The full text of the EU declaration of conformity is available at the following internet address www.hot-europe.com/support.
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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