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BEUDAMED

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21 results · 17ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 19 FDA classification 2 + More Filters

Country

United States 21 + More Countries

Classification

FDA Class 1 21 + More Classifications

FDA FEI Number

1000022662 19 1000113735 19 1000119305 19 1000160162 19 1000219637 19 1000221981 19 1000307631 19 1000402972 19 1000477302 19 1017294 19 1032347 19 1037007 19 1045254 19 1045834 19 1048735 19 1317628 19 1526534 19 1526611 19 1526711 19 1625507 19 + More FDA FEI Numbers

Regulation

Us FDA 21 + More Regulations

FDA Registration Number

1017294 19 1030489 19 1032347 19 1037007 19 1045254 19 1045834 19 1048735 19 1052728 19 1057421 19 1058084 19 1058322 19 1058584 19 1313525 19 1526534 19 1526611 19 1526711 19 1625507 19 1646747 19 1649518 19 1824199 19 + More FDA Registration Numbers

FDA K Number

K041985 1 K161514 1 K792028 1 K802503 1 K893499 1 K895738 1 K935584 1 K946332 1 K950337 1 K951526 1 K952609 1 K953096 1 K953370 1 K954912 1 K955294 1 K955704 1 K960853 1 K974232 1 + More FDA K Numbers

Bur, Ear, Nose And Throat

FDA classification

FDA Class 1 ·Bur, Ear, Nose And Throat

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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