QCG - BEUDAMED

BEUDAMED

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

Filters Classification: FDA Class 2 ×

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FDA 510(k) 961 FDA Pre-Market Approval 14 FDA classification 6 + More Filters

Country

United States 827 Canada 53 China 37 United Kingdom 25 Ireland 10 Japan 6 Switzerland 6 South Korea 4 Sweden 3 Taiwan 2 Denmark 1 Germany 1 Hong Kong 1 Israel 1 Italy 1 Jordan 1 Türkiye 1 Virgin Islands, British 1 + More Countries

Classification

FDA Class 2 981 + More Classifications

FDA FEI Number

3005569927 604 1000306617 602 3006305917 602 1000118544 601 1000126037 601 1313700 601 1832216 601 2025760 601 2246703 601 2250030 601 3000210620 601 3000719950 601 3001451797 601 3001452245 601 3002792284 601 3003075526 601 3003102569 601 3003347234 601 3003791481 601 3003917514 601 + More FDA FEI Numbers

Regulation

Us FDA 981 + More Regulations

FDA Registration Number

3005569927 604 2029372 602 3006305917 602 1313700 601 1645225 601 1649661 601 1832216 601 2025099 601 2025760 601 2030633 601 2031229 601 2060833 601 2087033 601 2246703 601 2250030 601 3002792284 601 3003791481 601 3003917514 601 3004132058 601 3004635103 601 + More FDA Registration Numbers

FDA K Number

K001215 1 K002049 1 K002944 1 K002946 1 K002947 1 K003856 1 K010522 1 K010593 1 K011075 1 K011270 1 K011550 1 K011551 1 K012215 1 K012284 1 K012358 1 K012559 1 K012864 1 K012943 1 K013069 1 K013070 1 + More FDA K Numbers

Test, Albumin Cobalt Binding

FDA classification

FDA Class 2 ·Test, Albumin Cobalt Binding

<1 …46 47 48 49 50 >

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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