JDK - BEUDAMED

BEUDAMED

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1,261 results · 24ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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

Country

United States 679 Denmark 393 Japan 44 China 39 Germany 20 Israel 20 France 19 Netherlands 16 Canada 12 Italy 4 United Kingdom 4 Switzerland 3 Australia 2 Austria 2 Finland 1 Norway 1 Sweden 1 Taiwan 1 + More Countries

Classification

FDA Class 2 1k + More Classifications

FDA FEI Number

3018094310 966 3000126629 924 3009077524 908 3009617712 906 3005877899 898 2011171 894 3001236277 893 2183744 892 3011050570 887 1000114111 885 1047843 884 3010703925 882 3010398867 871 3032109181 867 3011416394 864 3003076831 863 3001722928 861 3008496839 861 3000206435 859 3004977335 858 + More FDA FEI Numbers

Regulation

Us FDA 1k + More Regulations

FDA Registration Number

3018094310 966 3000126629 924 3009077524 908 3009617712 906 3005877899 898 2011171 894 1649518 893 2183744 892 3011050570 887 1054713 885 1047843 884 3010703925 882 3010398867 871 3032109181 867 3011416394 864 2032112 863 3001722928 861 3008496839 861 2030624 859 3004977335 858 + More FDA Registration Numbers

FDA K Number

K003718 1 K010528 1 K011443 1 K011998 1 K012255 1 K012278 1 K012462 1 K013014 1 K013663 1 K020344 1 K020836 1 K021719 1 K021765 1 K021788 1 K022218 1 K022615 1 K023647 1 K023908 1 K030608 1 K030767 1 + More FDA K Numbers

RTX 3371

FDA Class 2 ·Cardiovascular

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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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