IEC 60601-1

As medical product risk class 1 they are conform with the regulations (EU) 2017/745 (MDR) and IEC 60601-1. Other standards of the IEC 60601 series are not applicable to our products, regardless of their version.

Fraunhofer tested device

The Fraunhofer Institute confirms that the CIM mounting arms can be cleaned and disinfected simply by wiping.

CE marking

The mounting arms of CIM med® comply with the Regulation (EU) 2017/745 of the European Parliament and of the Council and are CE marked.

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