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BEUDAMED

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261 results · 40ms · Sources: EU EUDAMED, US FDA

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FDA classification 261 + More Filters

Country

United States 261 + More Countries

Classification

FDA Class 2 179 FDA Class 1 76 FDA Class 3 3 FDA Not Classified 2 FDA Unclassified 1 + More Classifications

FDA FEI Number

3001236905 109 3002902735 107 1643817 104 3007329020 101 3009888344 101 1928237 36 2183744 27 3037966040 27 1000512168 18 2011171 18 3035642068 18 3000717925 17 2020550 16 3002807795 16 3007475226 16 3011050570 16 3015173212 16 1000112877 15 1000112968 15 3014342096 15 + More FDA FEI Numbers

Regulation

Us FDA 261 + More Regulations

FDA Registration Number

1423537 109 9616088 107 1643817 104 3007329020 101 3009888344 101 1928237 36 2183744 27 3037966040 27 1061124 18 2011171 18 3035642068 18 1423395 17 2020550 16 3010202439 16 3011050570 16 3015173212 16 8010047 16 1054241 15 1055236 15 3014342096 15 + More FDA Registration Numbers

FDA K Number

Den090005 1 Den240018 1 K000032 1 K000036 1 K000044 1 K000046 1 K000074 1 K000151 1 K000153 1 K000170 1 K000197 1 K000198 1 K000200 1 K000202 1 K000216 1 K000228 1 K000241 1 K000245 1 K000250 1 K000296 1 + More FDA K Numbers

Radiology-Diagnostic Kit

FDA classification

FDA Class 2 ·Radiology-Diagnostic Kit

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

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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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