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BEUDAMED

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801 results · 19ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 3 ×

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FDA Pre-Market Approval 776 FDA 510(k) 22 FDA classification 3 + More Filters

Country

United States 801 + More Countries

Classification

FDA Class 3 801 + More Classifications

FDA FEI Number

1000118068 239 3003347293 239 3003407669 239 3006123332 239 3013840437 239 3015373820 239 3026391021 239 3030390308 239 3033486016 239 3037006441 239 2011068 238 3002807108 238 3003672980 238 3003707320 238 3004362706 238 3004423487 238 3005113652 238 3005975625 238 3006999111 238 3007093114 238 + More FDA FEI Numbers

Regulation

Us FDA 801 + More Regulations

FDA Registration Number

1000118068 239 2135225 239 3006123332 239 3013840437 239 3015373820 239 3026391021 239 3030390308 239 3033486016 239 3037006441 239 9710154 239 2011068 238 3002807108 238 3003672980 238 3003707320 238 3004362706 238 3004423487 238 3005113652 238 3005975625 238 3006999111 238 3007093114 238 + More FDA Registration Numbers

KIRSCHNER SELF-TAPPING ACETABULAR CUP

FDA Class 3 ·Orthopedic

<1 …37 38 39 40 41 >

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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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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