DRM - BEUDAMED

BEUDAMED

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141 results · 20ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 128 FDA classification 13 + More Filters

Country

United States 129 Malaysia 4 Canada 2 China 2 Chile 1 Dominican Republic 1 Israel 1 Taiwan 1 + More Countries

Classification

FDA Class 1 141 + More Classifications

FDA FEI Number

3007208013 89 3002750084 81 3012494290 73 1417592 58 3002677549 56 2027062 50 1000306431 48 3012421607 47 3017264244 47 3009171220 46 3026408938 46 3002808360 45 3009420946 45 3017604 45 3019261113 45 1821514 44 2416455 44 3001032747 44 3002809535 44 3005497907 44 + More FDA FEI Numbers

Regulation

Us FDA 141 + More Regulations

FDA Registration Number

3007208013 89 1836161 81 3012494290 73 1417592 58 9611959 56 2027062 50 2029275 48 3012421607 47 3017264244 47 3009171220 46 3026408938 46 3009420946 45 3017604 45 3019261113 45 9613083 45 1821514 44 2416455 44 3005497907 44 3022516928 44 3030499332 44 + More FDA Registration Numbers

FDA K Number

K010935 1 K021524 1 K021613 1 K022522 1 K040797 1 K043301 1 K050318 1 K071615 1 K090457 1 K142469 1 K151945 1 K182118 1 K191174 1 K760574 1 K770065 1 K770117 1 K770391 1 K771031 1 K780743 1 K780744 1 + More FDA K Numbers

Mercy Tape 2d And 3d Models

FDA classification

FDA Class 1 ·Mercy Tape 2d And 3d Models

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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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