FNJ - BEUDAMED

BEUDAMED

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1,421 results · 21ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 3 ×

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FDA Pre-Market Approval 1k FDA 510(k) 24 + More Filters

Country

United States 1k + More Countries

Classification

FDA Class 3 1k + More Classifications

FDA FEI Number

3003418325 508 2648209 448 1121308 444 1416980 427 3000204775 383 1213643 368 3014461810 365 1000120505 363 3006066614 363 3011689956 363 3012421607 363 1000138054 342 1000306431 316 3003120897 307 3010605677 303 3000215205 288 3010132111 270 3002807315 261 2528981 257 2011171 250 + More FDA FEI Numbers

Regulation

Us FDA 1k + More Regulations

FDA Registration Number

3003418325 508 2650143 448 1121308 444 1416980 427 2648988 383 1213643 368 3014461810 365 1223089 363 3006066614 363 3011689956 363 3012421607 363 1319639 342 2029275 316 3003120897 307 3010605677 303 2953359 288 3010132111 270 3002807315 261 2528981 257 2011171 250 + More FDA Registration Numbers

CPS ACETABULAR COMPONENT

FDA Class 3 ·Orthopedic

<1 …68 69 70 71 72 >

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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