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BEUDAMED

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3,341 results · 38ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 3k FDA classification 4 FDA Pre-Market Approval 1 + More Filters

Country

United States 3k Taiwan 46 Finland 21 Malaysia 21 Israel 18 Canada 17 China 13 Australia 9 India 6 Sweden 6 Thailand 6 Indonesia 5 South Korea 5 Hong Kong 4 Netherlands 4 Honduras 2 Mexico 2 British Indian Ocean Territory 1 Denmark 1 Germany 1 + More Countries

Classification

FDA Class 1 3k + More Classifications

FDA FEI Number

3012494290 1k 1417592 881 3007208013 853 3002750084 756 3012421607 730 3013557562 724 3001236905 675 3010131137 597 3015495690 596 1043214 583 3026408938 524 3005747797 501 1526534 498 1928237 491 3003418325 488 1220477 478 3015550354 474 2432235 473 2648727 470 3002806559 462 + More FDA FEI Numbers

Regulation

Us FDA 3k + More Regulations

FDA Registration Number

3012494290 1k 1417592 881 3007208013 853 1836161 756 3012421607 730 3013557562 724 1423537 675 3010131137 597 3015495690 596 1043214 583 3026408938 524 3011137372 500 1526534 498 1928237 491 3003418325 488 1220477 478 3015550354 474 2432235 473 2648727 470 9610126 462 + More FDA Registration Numbers

FDA K Number

Den150004 1 K820269 1 K853312 1 K872597 1 K874300 1 K874585 1 K882013 1 K885145 1 K885149 1 K890925 1 K913815 1 K921418 1 K933364 1 K944234 1 + More FDA K Numbers

SEMI-RECUMBENT CYCLES

FDA Class 1 ·Physical Medicine

<1 …164 165 166 167 168 >

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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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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