EWQ - BEUDAMED

BEUDAMED

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41 results · 20ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 40 FDA classification 1 + More Filters

Country

United States 38 United Kingdom 2 Malaysia 1 + More Countries

Classification

FDA Class 1 41 + More Classifications

FDA FEI Number

3006198300 18 3002806559 16 2432235 15 3002806560 15 3003795116 15 1827821 14 2050010 13 2050012 13 1000135102 12 1616487 12 1832216 12 3000215862 12 3004493545 12 3005333358 12 1000136573 11 1000206808 11 1181121 11 2250051 11 2517506 11 3002806809 11 + More FDA FEI Numbers

Regulation

Us FDA 41 + More Regulations

FDA Registration Number

3006198300 18 9610126 16 2432235 15 3003795116 15 9610529 15 1827821 14 2050010 13 2050012 13 1616487 12 1832216 12 2030861 12 2085064 12 3004493545 12 3005333358 12 1181121 11 1319681 11 2250051 11 2517506 11 3013660430 11 3014325803 11 + More FDA Registration Numbers

FDA K Number

K800669 1 K844765 1 + More FDA K Numbers

AMOILS EPITHELIAL SCRUBBER

FDA Class 1 ·Ophthalmic

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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