DIO - BEUDAMED

BEUDAMED

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

Filters Classification: FDA Class 3 ×

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FDA Pre-Market Approval 500 FDA 510(k) 21 + More Filters

Country

United States 521 + More Countries

Classification

FDA Class 3 521 + More Classifications

FDA FEI Number

1018233 389 3006082230 389 1028232 366 2124215 366 2183744 365 3002807111 365 1219930 364 2024024 364 3002807314 363 3010273872 363 1000121056 362 1000219637 362 1016427 362 1643817 362 2020394 362 2024168 362 2183870 362 3001451463 362 3001845648 362 3002095335 362 + More FDA FEI Numbers

Regulation

Us FDA 521 + More Regulations

FDA Registration Number

1018233 389 3006082230 389 1028232 366 2124215 366 2183744 365 3005941719 365 1219930 364 2024024 364 3002807314 363 3010273872 363 1000121056 362 1016427 362 1058584 362 1225687 362 1531050 362 1643817 362 2020394 362 2024168 362 2134265 362 2183870 362 + More FDA Registration Numbers

Stent, Iliac

FDA Pre-Market Approval

FDA Class 3 ·EXPRESS LD LLIAC PREMOUNTED STENT SYSTEM

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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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