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BEUDAMED

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21 results · 28ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 3 ×

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FDA Pre-Market Approval 20 FDA 510(k) 1 + More Filters

Country

United States 21 + More Countries

Classification

FDA Class 3 21 + More Classifications

FDA FEI Number

1721676 16 2011171 15 3002807314 15 2017233 14 1016427 13 1721686 13 3003528016 13 3000206435 12 3005580113 12 3007284313 12 3009526575 12 3008307705 11 3009380063 11 3012102437 11 1000114185 10 1000116158 10 1000135961 10 1820334 10 3001452571 10 3002534070 10 + More FDA FEI Numbers

Regulation

Us FDA 21 + More Regulations

FDA Registration Number

1721676 16 2011171 15 3002807314 15 2017233 14 1016427 13 1721686 13 9616099 13 2030624 12 3005580113 12 3007284313 12 3009526575 12 3008307705 11 3009380063 11 3012102437 11 1054811 10 1820334 10 2184009 10 2247858 10 2953200 10 3002808486 10 + More FDA Registration Numbers

Implant, Cochlear

FDA Pre-Market Approval

FDA Class 3 ·COMBO 40+ COCHLEAR IMPLANT SYSTEM

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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