ILP - BEUDAMED

BEUDAMED

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8,821 results · 59ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 9k FDA Pre-Market Approval 3 FDA classification 2 + More Filters

Country

United States 9k Israel 69 + More Countries

Classification

FDA Class 1 9k + More Classifications

FDA FEI Number

3007208013 3k 3002750084 3k 1417592 3k 3012494290 2k 1043214 2k 3005747797 2k 3001236905 2k 3013557562 2k 3004216008 2k 3003418325 2k 3005273623 2k 3006509795 2k 3026408938 2k 1000112877 2k 1000112968 2k 3002902735 1k 3004824601 1k 3012421607 1k 3005011024 1k 1119779 1k + More FDA FEI Numbers

Regulation

Us FDA 9k + More Regulations

FDA Registration Number

3007208013 3k 1836161 3k 1417592 3k 3012494290 2k 1043214 2k 3011137372 2k 1423537 2k 3013557562 2k 8040278 2k 3003418325 2k 3005273623 2k 8030607 2k 3026408938 2k 1054241 2k 1055236 2k 9616088 1k 3004824601 1k 3012421607 1k 3005011024 1k 1119779 1k + More FDA Registration Numbers

FDA K Number

K761117 1 K770032 1 K781204 1 K810452 1 K811483 1 K811487 1 K821644 1 K823608 1 K823609 1 K823610 1 K823612 1 K823613 1 K823614 1 K823615 1 K823616 1 K823617 1 K823624 1 K823625 1 K831546 1 K840112 1 + More FDA K Numbers

EPILATOR, MULTIPLE NEEDLE-MODEL EM-20

FDA Class 1 ·General, Plastic Surgery

<1 …438 439 440 441 442 >

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

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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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