K033458 - BEUDAMED

BEUDAMED

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1 results · 21ms · Sources: EU EUDAMED, US FDA

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FDA FEI Number

1028232 1 1035166 1 1928237 1 2017865 1 2124215 1 2182208 1 2183744 1 2183787 1 2648729 1 2649622 1 3000203000 1 3002618605 1 3002806500 1 3003574398 1 3004785273 1 3005029049 1 3006705815 1 3008377825 1 3008973940 1 3008988055 1 + More FDA FEI Numbers

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FDA Registration Number

1028232 1 1035166 1 1061927 1 1928237 1 2017865 1 2032521 1 2124215 1 2182208 1 2183744 1 2183787 1 2648729 1 2649622 1 3004785273 1 3005029049 1 3006705815 1 3008494315 1 3008973940 1 3008988055 1 3009380063 1 3013288201 1 + More FDA Registration Numbers

VS-1 LEAD EXT. 033-302, 4.75MM 033-260, 033-458

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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