EU Representative for MDR 2017/745 and IVDR 2017/7..

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EU Representative for MDR 2017/745 and IVDR 2017/746

According to EU MDR, 2017/745 and IVDR 2017/746, an European Authorized Representative is mandatory for Non EU manufacturers wishing to sell medical devices

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European Authorized Representative | EU Rep Services

According to EU MDR, 2017/745 and IVDR 2017/746, an European Authorized Representative is mandatory for Non EU manufacturers wishing to sell medical devices

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European Authorized Representative | EU Rep Services

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