HME - BEUDAMED

BEUDAMED

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1,701 results · 22ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 1k FDA classification 204 + More Filters

Country

United States 2k Canada 10 United Kingdom 5 Australia 3 Taiwan 2 Argentina 1 Italy 1 Japan 1 Mexico 1 South Korea 1 Sweden 1 + More Countries

Classification

FDA Class 1 2k + More Classifications

FDA FEI Number

1000122536 558 3017539597 441 3006236690 429 3004107906 413 3005182159 408 1114298 403 1318354 390 3006158025 386 3008624479 386 3005182157 385 3008496303 385 3013221738 383 3014588186 371 3010512490 370 3033849281 370 1048735 368 2022379 368 3015715780 368 3036495174 368 1000123180 367 + More FDA FEI Numbers

Regulation

Us FDA 2k + More Regulations

FDA Registration Number

1528450 558 3017539597 441 3006236690 429 3004107906 413 3005182159 408 1114298 403 1318354 390 3006158025 386 3008624479 386 3005182157 385 3008496303 385 3013221738 383 3014588186 371 3010512490 370 3033849281 370 1048735 368 2022379 368 3015715780 368 3036495174 368 1123137 367 + More FDA Registration Numbers

FDA K Number

K000527 1 K000528 1 K000578 1 K013097 1 K020816 1 K021150 1 K022512 1 K023046 1 K030528 1 K033983 1 K040077 1 K050063 1 K051115 1 K051409 1 K060264 1 K061793 1 K061805 1 K063295 1 K083878 1 K100684 1 + More FDA K Numbers

Methyl Orange

FDA classification

FDA Class 1 ·Methyl Orange

<1 …82 83 84 85 86 >

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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