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Are you ready for Brexit? Do you have a Brexit contingency plan?

You may need either an EU/EC European authorized representative based in EU-27 countries or a UK authorised representative (so-called "UK Responsible Person") based in UK, or may even need both EU & UK representatives, depending on different brexit scenarios.

Register/Notify your MD-Medical Devices & IVD-In Vitro Diagnostic Medical
Devices with MHRA in UK & other EEA (EU/EFTA) authorities by world-leading
consultancy- Wellkang team based in both UK (England) & EU-27 (Ireland).

Wellkang team can help you under all Brexit scenarios!
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AIMD-Active Implantable Medical Devices: Conformity Assessment Routes

Flow Chart of AIMD


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FAQ/Q&A: Questions and Answers about CE Marking of Medical Devices About CE Marking:

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