K182345 - BEUDAMED

BEUDAMED

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781 results · 41ms · Sources: EU EUDAMED, US FDA

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FDA 510(k) 702 FDA registration 40 FDA classification 35 FDA UDI 4 + More Filters

Country

United States 768 Canada 2 Japan 2 Taiwan 2 United Kingdom 2 Australia 1 China 1 Ireland 1 Israel 1 Malaysia 1 + More Countries

Classification

FDA Class 1 731 FDA Class 2 6 + More Classifications

FDA FEI Number

2182345 763 1043214 648 3006076154 593 3017264244 593 1000123222 575 1000208624 563 1417592 538 3010452421 524 1026765 504 3004605321 494 3012316249 484 3005273623 450 3006336810 442 3004824601 428 3026408938 424 3006400320 408 3007774549 400 1000143485 399 3007208013 399 3002750084 395 + More FDA FEI Numbers

Regulation

Us FDA 781 + More Regulations

FDA Registration Number

2182345 763 1043214 648 3017264244 593 9616086 593 1123071 575 1060680 563 1417592 538 3010452421 524 1026765 504 3004605321 494 3012316249 484 3005273623 450 3006336810 442 3004824601 428 3026408938 424 3006400320 408 3007774549 400 1422443 399 3007208013 399 1836161 395 + More FDA Registration Numbers

FDA K Number

K001742 1 K010039 1 K010184 1 K010191 1 K010403 1 K010553 1 K010644 1 K010818 1 K011240 1 K011616 1 K011738 1 K012014 1 K012205 1 K012210 1 K012324 1 K012975 1 K013040 1 K013203 1 K013239 1 K013244 1 + More FDA K Numbers

Instrument, Manual, Surgical, General Use

FDA classification

FDA Class 1 ·Instrument, Manual, Surgical, General Use

<1 …36 37 38 39 40 >

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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