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Regulation (EU) 2017/745 on Medical Devices | EU MDR

CE marking by product type

Regulation (EU) 2017 / 745

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Testing and certification laboratory accredited for CE Marking.

We help manufacturers validate their products, meet regulatory requirements, and securely access the European and international market.

Interactive guide CE Marking

ENAC accredited laboratory nº 51/LE147 in accordance with ISO/IEC 17025

CE marking

> Obligations
> Requirements
> Declaration of conformity

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