JKC - BEUDAMED

BEUDAMED

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41 results · 16ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 41 + More Filters

Country

United States 24 Taiwan 5 Canada 3 Australia 2 Thailand 2 United Kingdom 2 Netherlands 1 Russian Federation 1 South Korea 1 + More Countries

Classification

FDA Class 2 41 + More Classifications

FDA FEI Number

3000210620 13 1000306617 12 1417592 12 1832216 12 2244821 12 3003917514 12 3005670738 12 1000126037 11 2432235 11 3001451797 11 3006198300 11 3009238284 11 3012494290 11 3012725363 11 3005984081 10 3006305917 10 3012073813 10 3027519599 10 1827821 9 2246703 9 + More FDA FEI Numbers

Regulation

Us FDA 41 + More Regulations

FDA Registration Number

2030633 13 1417592 12 1832216 12 2029372 12 2244821 12 3003917514 12 3005360469 12 1649661 11 2432235 11 3006198300 11 3009238284 11 3012494290 11 3012725363 11 3025672 11 3005984081 10 3006305917 10 3012073813 10 3027519599 10 1827821 9 2025099 9 + More FDA Registration Numbers

ONE STEP PREGNANCY TEST

FDA Class 2 ·Clinical Chemistry

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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