JOX - BEUDAMED

BEUDAMED

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3,821 results · 40ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 4k FDA classification 6 FDA Pre-Market Approval 3 + More Filters

Country

United States 4k Taiwan 47 Malaysia 28 Canada 21 Finland 21 Israel 19 China 13 Australia 10 Sweden 9 South Korea 8 Thailand 8 Indonesia 6 India 5 Netherlands 5 Hong Kong 4 Honduras 2 Japan 2 Mexico 2 New Zealand 2 Virgin Islands, British 2 + More Countries

Classification

FDA Class 1 4k + More Classifications

FDA FEI Number

3012494290 1k 1417592 1k 3007208013 952 3012421607 850 3013557562 838 3002750084 835 3001236905 785 3010131137 686 1043214 661 3015495690 639 1928237 596 3026408938 596 1220477 573 2648727 564 3003418325 562 2432235 561 3005747797 559 3015550354 557 3002806559 555 1526534 546 + More FDA FEI Numbers

Regulation

Us FDA 4k + More Regulations

FDA Registration Number

3012494290 1k 1417592 1k 3007208013 952 3012421607 850 3013557562 838 1836161 835 1423537 785 3010131137 686 1043214 661 3015495690 639 1928237 596 3026408938 596 1220477 573 2648727 564 3003418325 562 2432235 561 3011137372 559 3015550354 557 9610126 555 1526534 546 + More FDA Registration Numbers

FDA K Number

K792306 1 K800430 1 K881885 1 K891927 1 K920131 1 K933449 1 K934683 1 K935472 1 K942018 1 K943632 1 K943680 1 K944294 1 K944348 1 K944386 1 K944387 1 K944388 1 K944389 1 K944390 1 K944521 1 K945867 1 + More FDA K Numbers

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FDA Class 1 ·General Hospital

<1 …188 189 190 191 192 >

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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