EFS - BEUDAMED

BEUDAMED

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2,461 results · 28ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 2k FDA classification 190 FDA Pre-Market Approval 2 + More Filters

Country

United States 2k Spain 22 United Kingdom 18 Taiwan 13 Germany 11 Canada 10 China 8 Denmark 6 Hong Kong 6 Israel 5 Netherlands 4 Australia 3 Greece 2 South Korea 2 Egypt 1 France 1 India 1 Japan 1 New Zealand 1 Sweden 1 + More Countries

Classification

FDA Class 1 2k + More Classifications

FDA FEI Number

3012494290 2k 3009307953 1k 3001620590 1k 1526534 1k 1000140463 1k 3007367732 1k 3002807554 1k 3005581270 1k 3003610251 1k 3016630774 1k 3001739169 1k 3037024831 1k 3007694978 1k 1044692 1k 1000113652 1k 2240713 1k 3002196172 1k 3003303986 1k 3005465494 1k 3005650109 1k + More FDA FEI Numbers

Regulation

Us FDA 2k + More Regulations

FDA Registration Number

3012494290 2k 3009307953 1k 3001620590 1k 1526534 1k 1056339 1k 3007367732 1k 3005581270 1k 9612197 1k 3003610251 1k 3016630774 1k 1063974 1k 3037024831 1k 3007694978 1k 1044692 1k 1052698 1k 1724310 1k 2240713 1k 3003303986 1k 3005465494 1k 3005650109 1k + More FDA Registration Numbers

FDA K Number

K000108 1 K001493 1 K002131 1 K003204 1 K003558 1 K011544 1 K012532 1 K013987 1 K020706 1 K020707 1 K020717 1 K021172 1 K021687 1 K021789 1 K021867 1 K022133 1 K022713 1 K022743 1 K022845 1 K023232 1 + More FDA K Numbers

Oral Irrigation Kit

FDA classification

FDA Class 1 ·Oral Irrigation Kit

<1 …120 121 122 123 124 >

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

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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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