Compumedics Germany GmbH - BEUDAMED

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1 results · 58ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 1 + More Filters

Country

Germany 1 + More Countries

Classification

FDA Class 2 1 + More Classifications

FDA FEI Number

1000080301 1 1000114111 1 1000124215 1 1000139867 1 1000219637 1 1000263641 1 1000269286 1 1000306431 1 1000601180 1 1037998 1 1045254 1 1416980 1 1450908 1 1528028 1 1643817 1 1826555 1 1937397 1 2183744 1 2221819 1 2518586 1 + More FDA FEI Numbers

Regulation

Us FDA 1 + More Regulations

FDA Registration Number

1000269286 1 1000601180 1 1037998 1 1045254 1 1054713 1 1058584 1 1062741 1 1066270 1 1066427 1 1126271 1 1416980 1 1450908 1 1528028 1 1643817 1 1649518 1 1826555 1 1937397 1 2029275 1 2031044 1 2032350 1 + More FDA Registration Numbers

DOPPLER-BOX

FDA Class 2 ·Radiology

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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