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BEUDAMED

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21 results · 18ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 20 FDA classification 1 + More Filters

Country

Malaysia 10 Canada 5 United States 4 Indonesia 1 United Kingdom 1 + More Countries

Classification

FDA Class 1 21 + More Classifications

FDA FEI Number

1220477 14 3013557562 14 3010600155 13 1000099913 11 1000124109 11 1000148701 11 1000153304 11 1000154563 11 1000254914 11 1000266564 11 1043549 11 1119294 11 1221744 11 1250045 11 1319302 11 1417592 11 1928237 11 2183301 11 2648727 11 2938651 11 + More FDA FEI Numbers

Regulation

Us FDA 21 + More Regulations

FDA Registration Number

1220477 14 3013557562 14 3010600155 13 1000254914 11 1000266564 11 1043549 11 1119294 11 1219103 11 1221744 11 1250045 11 1319302 11 1417592 11 1423537 11 1928237 11 2024980 11 2084709 11 2087418 11 2183301 11 2437780 11 2648727 11 + More FDA Registration Numbers

FDA K Number

K780230 1 + More FDA K Numbers

Board, Bed

FDA classification

FDA Class 1 ·Board, Bed

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

BEUDAMED

A better medical device search engine by OpenRegulatory.

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BEUDAMED

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EU MDR

EU MDR Medical Devices EU MDR Active Medical Devices EU MDR Class I Medical Devices EU MDR Class I Software Devices EU MDR Class IIa Medical Devices EU MDR Class IIa Software Devices EU MDR Class IIb Medical Devices EU MDR Class IIb Software Devices EU MDR Class III Medical Devices EU MDR Class III Software Devices EU MDR Implantable Medical Devices EU MDR Measuring Function Medical Devices EU MDR Software Medical Devices

EU IVDR

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

FDA

FDA Medical Devices FDA Class I Medical Devices FDA Class II Medical Devices FDA Class III Medical Devices

By Country

EU IVDR Medical Devices from China EU IVDR Medical Devices from France EU IVDR Medical Devices from Germany EU IVDR Medical Devices from Romania EU IVDR Medical Devices from United States EU MDR Medical Devices from China EU MDR Medical Devices from Egypt EU MDR Medical Devices from Finland EU MDR Medical Devices from France EU MDR Medical Devices from Germany EU MDR Medical Devices from Italy EU MDR Medical Devices from Pakistan EU MDR Medical Devices from Poland EU MDR Medical Devices from Spain EU MDR Medical Devices from Türkiye EU MDR Medical Devices from United Kingdom EU MDR Medical Devices from United States

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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