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BEUDAMED

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641 results · 24ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 582 FDA classification 59 + More Filters

Country

United States 598 United Kingdom 15 China 9 Canada 6 New Zealand 5 Israel 3 Australia 1 Finland 1 Germany 1 Pakistan 1 South Korea 1 + More Countries

Classification

FDA Class 1 641 + More Classifications

FDA FEI Number

3007208013 309 3002750084 303 3006509795 294 1417592 275 3004824601 264 3006513362 227 1043214 214 3013846070 186 1928237 185 3014421917 178 1000143485 166 1000137528 164 3004574120 159 3004216008 153 1824206 148 2648727 145 3007289408 145 3013557562 144 1000123222 140 3026408938 140 + More FDA FEI Numbers

Regulation

Us FDA 641 + More Regulations

FDA Registration Number

3007208013 309 1836161 303 8030607 294 1417592 275 3004824601 264 3006513362 227 1043214 214 3013846070 186 1928237 185 3014421917 178 1422443 166 2435946 164 9613910 159 8040278 153 1824206 148 2648727 145 3007289408 145 3013557562 144 1123071 140 3026408938 140 + More FDA Registration Numbers

FDA K Number

Den110009 1 Den150004 1 K010981 1 K011827 1 K030829 1 K042145 1 K050313 1 K052770 1 K062061 1 K072882 1 K090138 1 K101109 1 K102101 1 K103817 1 K110858 1 K113355 1 K113357 1 K130752 1 K131585 1 K141208 1 + More FDA K Numbers

Dynamometer, Nonpowered

FDA classification

FDA Class 1 ·Dynamometer, Nonpowered

<1 …29 30 31 32 33 >

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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