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BEUDAMED

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541 results · 33ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 539 FDA classification 2 + More Filters

Country

United States 341 Malaysia 144 Hong Kong 19 United Kingdom 12 Taiwan 8 China 6 Philippines 3 Canada 2 Japan 2 India 1 Ireland 1 Madagascar 1 South Korea 1 + More Countries

Classification

FDA Class 1 541 + More Classifications

FDA FEI Number

1417592 302 3012421607 288 3001236905 271 3013557562 250 2648727 236 3014421917 232 1928237 211 3006066614 208 3026297922 208 3014683120 206 1220477 204 2183301 204 3012494290 202 1319302 200 3010131137 200 3014268334 200 3008875470 195 3010220595 195 3011209798 194 3010862763 193 + More FDA FEI Numbers

Regulation

Us FDA 541 + More Regulations

FDA Registration Number

1417592 302 3012421607 288 1423537 271 3013557562 250 2648727 236 3014421917 232 1928237 211 3006066614 208 3026297922 208 3014683120 206 1220477 204 2183301 204 3012494290 202 1319302 200 3010131137 200 3014268334 200 2024980 195 3010220595 195 3011209798 194 3010864832 193 + More FDA Registration Numbers

FDA K Number

K142469 1 K191174 1 K800550 1 K860554 1 + More FDA K Numbers

PROSTATE-63 CANCER DIAGNOSTIC TEST

FDA Class 1 ·Hematology

<1 …24 25 26 27 28 >

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

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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