K200190 - BEUDAMED

BEUDAMED

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1 results · 23ms · Sources: EU EUDAMED, US FDA

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1000127185 1 1000140026 1 1000148701 1 1000305720 1 1000524572 1 1218058 1 1220908 1 1317188 1 1720929 1 1921846 1 1930027 1 2112020 1 3000126629 1 3000215273 1 3001236905 1 3001451571 1 3002714378 1 3003491392 1 3003521780 1 3003537036 1 + More FDA FEI Numbers

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1218058 1 1219103 1 1220908 1 1223925 1 1317188 1 1320894 1 1423537 1 1423662 1 1720929 1 1921846 1 1930027 1 2112020 1 2132111 1 3000126629 1 3002714378 1 3003521780 1 3003537036 1 3003800159 1 3003867964 1 3004035727 1 + More FDA Registration Numbers

BIO-DETEK ELECTRODE ADAPTER, MODEL R2001-90

FDA Class 3 ·Cardiovascular

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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