OBT - BEUDAMED

BEUDAMED

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4,541 results · 33ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 4k FDA classification 207 FDA Pre-Market Approval 50 + More Filters

Country

United States 4k China 170 Germany 88 United Kingdom 75 Canada 66 Denmark 49 Japan 48 Sweden 48 Malaysia 42 Israel 39 Australia 37 South Korea 35 Taiwan 24 India 23 Netherlands 18 Thailand 17 Switzerland 14 Italy 10 France 9 Ireland 7 + More Countries

Classification

FDA Class 2 5k + More Classifications

FDA FEI Number

1216677 2k 1043214 1k 1000112877 1k 1000112968 1k 1000138054 1k 3003040625 1k 1820334 1k 3013557562 1k 3010687142 999 3012494290 998 3015976667 992 3004111573 985 1000306431 972 1825146 948 2938651 938 3002808001 917 3014279513 916 3001451571 913 3007475226 913 2020550 912 + More FDA FEI Numbers

Regulation

Us FDA 5k + More Regulations

FDA Registration Number

1216677 2k 1043214 1k 1054241 1k 1055236 1k 1319639 1k 2320762 1k 1820334 1k 3013557562 1k 3003896222 999 3012494290 998 3015976667 992 3004111573 985 2029275 972 1825146 948 2938651 938 3014279513 916 1320894 913 3010202439 913 2020550 912 9611102 907 + More FDA Registration Numbers

FDA K Number

Den000006 1 Den020001 1 Den040009 1 Den060006 1 Den090004 1 Den090011 1 Den120015 1 Den130040 1 Den140010 1 Den150008 1 Den150028 1 Den150053 1 Den160005 1 Den160014 1 Den170052 1 Den200026 1 Den210034 1 Den220083 1 Den230043 1 K000026 1 + More FDA K Numbers

Perineometer

FDA classification

FDA Class 2 ·Perineometer

<1 …224 225 226 227 228 >

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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