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BEUDAMED

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721 results · 18ms · Sources: EU EUDAMED, US FDA

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FDA Pre-Market Approval 718 FDA 510(k) 2 FDA classification 1 + More Filters

Country

United States 721 + More Countries

Classification

FDA Class 3 721 + More Classifications

FDA FEI Number

2011171 433 3002807314 433 2024168 431 3004091615 431 3004635528 431 2183744 429 1016427 425 3003528016 425 3010432890 380 2124215 335 3002806565 326 1219930 320 1643817 320 2183870 320 2024024 300 3002807036 289 3003473227 289 3003956144 289 3007215228 289 3010079067 289 + More FDA FEI Numbers

Regulation

Us FDA 721 + More Regulations

FDA Registration Number

2011171 433 3002807314 433 2024168 431 2939561 431 3004091615 431 2183744 429 1016427 425 9616099 425 3010432890 380 2124215 335 9681260 326 1219930 320 1643817 320 2183870 320 2024024 300 1424778 289 3003956144 289 3010079067 289 3010173425 289 3011471056 289 + More FDA Registration Numbers

OSCOR MEDICAL IMPLANTABLE PACING LEAD, RETRACTABLE

FDA Class 3 ·Cardiovascular

<1 …33 34 35 36 37 >

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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