Risk management is at the heart of medical device safety assessment and a manufacturer is required to perform an assessment based on the requirements of the standard in combination with the risk identified by the manufacturer. It would not be useless for any electromedical product that could be exposed to RFID to include these tests for immunity to specific frequencies and modulations in its assessment.
Risk management is at the heart of medical device safety assessment and a manufacturer is required to perform an assessment based on the requirements of the standard in combination with the risk identified by the manufacturer. It would not be useless for any electromedical product that could be exposed to RFID to include these tests for immunity to specific frequencies and modulations in its assessment.
Dear customers,
In the current context, we are adapting our organization to integrate the measures taken by the authorities while maintaining our commitments to you.
Our priority is to ensure the continuity of the missions we carry out for your company, while taking all necessary measures to protect our employees.
EMC joins the Emitech Group
The Emitech Group is celebrating its 30th anniversary this year and we will be pleased to start 2019 wih a new exceptional acquisition, both in terms of size and ambition: EMC France joined the Emitech Group on March 28.
Marquage CE - Date d'application des nouvelles directives CEM / Basse Tension et la directive RED
Le marquage CE d'un produit atteste qu'il satisfait à l'ensemble des directives lui étant applicables.
Dès lors que des directives évoluent, les informations traitant des dates d'applicabilités et des périodes de transition (le cas échéant) deviennent de première importance.
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