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Medical Device Services

Across the highly regulated medical devices industry, ISO13485 is a globally recognised  baseline for compliance. DEKRA Certification UK Ltd intends to offer quality management certification to ISO13485, ISO9001 and MDSAP, in addition to product UKCA and CE certification, in collaboration with our European notified bodies in Netherlands and Germany.

The DEKRA UK team of medical device experts is field supported by an extensive network of competence throughout global DEKRA to help you access worldwide markets for all medical devices, including in vitro diagnostic devices.
Please see the product pages below for more information on DEKRA services.