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BEUDAMED

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

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FDA Pre-Market Approval 340 FDA 510(k) 1 + More Filters

Country

United States 341 + More Countries

Classification

FDA Class 3 341 + More Classifications

FDA FEI Number

3002807314 159 2011171 156 3006946276 153 1119279 121 1317628 121 1610287 121 3002807944 121 2124215 88 3009380063 88 3010273872 88 1000121056 87 2183744 87 3001451463 87 3001452571 87 3002095335 87 3002806434 87 3002806565 87 1000125183 86 2022180 86 2916205 86 + More FDA FEI Numbers

Regulation

Us FDA 341 + More Regulations

FDA Registration Number

3002807314 159 2011171 156 3006946276 153 1119279 121 1313525 121 1610287 121 9681121 121 2124215 88 3009380063 88 3010273872 88 1000121056 87 1225687 87 2134265 87 2183744 87 2953200 87 9612164 87 9681260 87 2022180 86 2028492 86 2916205 86 + More FDA Registration Numbers

Intraocular Lens

FDA Pre-Market Approval

FDA Class 3 ·MODEL PC-36CNB (TIER A)

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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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