K002002 - BEUDAMED

BEUDAMED

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1 results · 20ms · Sources: EU EUDAMED, US FDA

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FDA FEI Number

1000122536 1 1000123180 1 1048735 1 1114298 1 1318354 1 2022379 1 3002806725 1 3002836339 1 3004107906 1 3005182157 1 3005182159 1 3005875593 1 3006158025 1 3006236690 1 3008496303 1 3008624479 1 3010512490 1 3013221738 1 3014015490 1 3014588186 1 + More FDA FEI Numbers

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1048735 1 1114298 1 1123137 1 1226230 1 1318354 1 1528450 1 2022379 1 3004107906 1 3005182157 1 3005182159 1 3005875593 1 3006158025 1 3006236690 1 3008496303 1 3008624479 1 3010512490 1 3013221738 1 3014015490 1 3014588186 1 3015715780 1 + More FDA Registration Numbers

DULBECCO'S MODIFIED EAGLE'S MEDIUM, NO. 200-2002

FDA Class 1 ·Hematology

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

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EU IVDR In Vitro Diagnostic Devices EU IVDR Class A In Vitro Diagnostic Devices EU IVDR Class A Software Devices EU IVDR Class B In Vitro Diagnostic Devices EU IVDR Class B Software Devices EU IVDR Class C In Vitro Diagnostic Devices EU IVDR Class C Software Devices EU IVDR Class D In Vitro Diagnostic Devices EU IVDR Class D Software Devices EU IVDR Instrument Devices EU IVDR Kit Devices EU IVDR Reagent Devices EU IVDR Software Devices

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Notified Bodies

BSI Group The Netherlands B.V. DEKRA Certification B.V. DNV Product Assurance AS POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. SGS Belgium NV TÜV Rheinland LGA Products GmbH TÜV SÜD Product Service GmbH UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş.

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