K043507 - BEUDAMED

BEUDAMED

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761 results · 50ms · Sources: EU EUDAMED, US FDA

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FDA 510(k) 686 FDA registration 40 FDA classification 34 FDA UDI 1 + More Filters

Country

United States 707 Germany 32 Canada 6 United Kingdom 3 Australia 2 France 2 Japan 2 China 1 India 1 Ireland 1 Malaysia 1 Mexico 1 Pakistan 1 Switzerland 1 + More Countries

Classification

FDA Class 1 715 FDA Class 2 5 + More Classifications

FDA FEI Number

3000041196 747 3007208013 715 3002806315 714 3004216008 709 3003418325 708 3005809810 708 3002750084 707 3003499455 700 3003944071 700 1421101 699 3005528784 698 3019261113 695 1000115048 693 3002806816 693 1720747 692 3005747797 688 3010041511 688 1527821 687 1417592 685 3008782585 685 + More FDA FEI Numbers

Regulation

Us FDA 761 + More Regulations

FDA Registration Number

8043507 747 3007208013 715 9610612 714 8040278 709 3003418325 708 3005809810 708 1836161 707 8040233 700 9710524 700 1421101 699 3005528784 698 3019261113 695 1421879 693 9611283 693 1720747 692 3010041511 688 3011137372 688 1527821 687 1417592 685 9611112 685 + More FDA Registration Numbers

FDA K Number

K000273 1 K000464 1 K000851 1 K001178 1 K001339 1 K001897 1 K002268 1 K002297 1 K002874 1 K003209 1 K003231 1 K003258 1 K003369 1 K003487 1 K003507 1 K003591 1 K003744 1 K003965 1 K004008 1 K010184 1 + More FDA K Numbers

Tray, Surgical, Instrument

FDA classification

FDA Class 1 ·Tray, Surgical, Instrument

<1 …35 36 37 38 39 >

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

BEUDAMED

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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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