Model Solution - BEUDAMED

BEUDAMED

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121 results · 68ms · Sources: EU EUDAMED, US FDA

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FDA registration 53 FDA 510(k) 29 FDA UDI 26 FDA Pre-Market Approval 13 + More Filters

Country

United States 82 Belgium 6 Malaysia 6 Ukraine 6 China 5 Germany 4 Colombia 2 Sweden 2 Switzerland 2 Taiwan 2 Australia 1 Netherlands 1 South Korea 1 Spain 1 + More Countries

Classification

FDA Class 2 22 FDA Class 3 11 FDA Class 1 6 FDA Unclassified 1 + More Classifications

FDA FEI Number

3006759904 13 3002806559 12 1181121 11 1219029 11 1717966 11 3026408938 11 1220972 10 1616487 10 1720929 10 1832216 10 2050012 10 2432235 10 3006198300 10 3007662974 10 3010131137 10 3012104670 10 3015997711 10 1000122044 9 1000135102 9 1219913 9 + More FDA FEI Numbers

Regulation

Us FDA 121 + More Regulations

FDA Registration Number

3009171251 13 9610126 12 1181121 11 1219029 11 1717966 11 3026408938 11 1220972 10 1616487 10 1720929 10 1832216 10 2050012 10 2432235 10 3006198300 10 3007662974 10 3010131137 10 3012104670 10 3015997711 10 1064608 9 1219913 9 1220649 9 + More FDA Registration Numbers

Twist Drills

FDA registration

NOBEL BIOCARE DISTRIBUTION CENTER BV·1 product·🇳🇱 Netherlands

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

BEUDAMED

A better medical device search engine by OpenRegulatory.

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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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