ITY - BEUDAMED

BEUDAMED

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901 results · 27ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

Filter by

FDA 510(k) 882 FDA classification 19 + More Filters

Country

United States 663 China 97 Taiwan 59 Italy 51 Japan 7 Malaysia 4 Canada 3 Switzerland 3 Vietnam 3 India 2 Philippines 2 South Korea 2 Cambodia 1 Egypt 1 Hong Kong 1 Mexico 1 Netherlands 1 + More Countries

Classification

FDA Class 1 901 + More Classifications

FDA FEI Number

1417592 316 3012421607 278 3014421917 264 3013557562 262 2648727 259 3012494290 240 1928237 226 3007502227 223 1000137528 215 3008875470 215 1043214 207 3007289408 202 1250045 193 3001236905 192 2939388 189 3005558160 187 3003199637 186 3007838093 186 3011209798 186 3015495690 185 + More FDA FEI Numbers

Regulation

Us FDA 901 + More Regulations

FDA Registration Number

1417592 316 3012421607 278 3014421917 264 3013557562 262 2648727 259 3012494290 240 1928237 226 3007502227 223 2024980 215 2435946 215 1043214 207 3007289408 202 1250045 193 1423537 192 2939388 189 3005558160 187 3003199637 186 3007838093 186 3011209798 186 3015495690 185 + More FDA Registration Numbers

FDA K Number

K000052 1 K000178 1 K000179 1 K000295 1 K000421 1 K000896 1 K000971 1 K001047 1 K001049 1 K001239 1 K001274 1 K001326 1 K001343 1 K001924 1 K001959 1 K002192 1 K002593 1 K002933 1 K003019 1 K003063 1 + More FDA K Numbers

VICTORY EYEWEAR CO

FDA Class 1 ·Ophthalmic

<1 …42 43 44 45 46 >

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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