Medical

ISO 20417:2021 Medical devices – Information to be supplied by the manufacturer
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Application of transitional provisions for certification of class D in vitro diagnostic medical devices according to Regulation 2017/746
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Medical devices: EU regulations for MDR and IVDR (Northern Ireland)
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Guidance on state of the art of COVID-19 rapid antibody tests
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How to be MDR compliant in the absence of EUDAMED
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Management of Legacy Devices in Eudamed
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ISO 10993-23:2021 Biological evaluation of medical devices – Part 23: Tests for irritation
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