PHO - BEUDAMED

BEUDAMED

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7,821 results · 73ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

Filter by

FDA 510(k) 8k FDA classification 158 FDA Pre-Market Approval 1 + More Filters

Country

United States 5k Malaysia 1k China 705 Taiwan 175 Indonesia 138 Thailand 136 India 99 Canada 49 Hong Kong 38 Vietnam 37 United Kingdom 24 Sri Lanka 18 Mali 16 Switzerland 11 Madagascar 10 Philippines 9 Ireland 8 Netherlands 7 Israel 6 Mexico 6 + More Countries

Classification

FDA Class 1 8k + More Classifications

FDA FEI Number

1417592 6k 3012421607 6k 3013557562 6k 3014421917 5k 2648727 5k 3001236905 5k 1928237 5k 3011209798 5k 3003199637 5k 2939388 5k 3003529075 4k 3010131137 4k 1250045 4k 3010363542 4k 3012104670 4k 3015997711 4k 3005558160 4k 3008875470 4k 1319302 4k 3014268334 4k + More FDA FEI Numbers

Regulation

Us FDA 8k + More Regulations

FDA Registration Number

1417592 6k 3012421607 6k 3013557562 6k 3014421917 5k 2648727 5k 1423537 5k 1928237 5k 3011209798 5k 3003199637 5k 2939388 5k 3003529075 4k 3010131137 4k 1250045 4k 3010363542 4k 3012104670 4k 3015997711 4k 3005558160 4k 2024980 4k 1319302 4k 3014268334 4k + More FDA Registration Numbers

FDA K Number

K000050 1 K000058 1 K000071 1 K000090 1 K000138 1 K000139 1 K000141 1 K000142 1 K000143 1 K000145 1 K000156 1 K000165 1 K000166 1 K000178 1 K000179 1 K000217 1 K000223 1 K000226 1 K000295 1 K000323 1 + More FDA K Numbers

Mercy Tape 2d And 3d Models

FDA classification

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

<1 …388 389 390 391 392 >

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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