K043010 - BEUDAMED

BEUDAMED

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

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FDA 510(k) 507 FDA classification 15 FDA registration 15 FDA UDI 4 + More Filters

Country

United States 487 Canada 15 Taiwan 13 United Kingdom 6 Hong Kong 3 Indonesia 3 Israel 2 Switzerland 2 Virgin Islands, British 2 Australia 1 Austria 1 China 1 Japan 1 Mexico 1 Netherlands 1 New Zealand 1 Spain 1 + More Countries

Classification

FDA Class 1 516 FDA Class 2 6 + More Classifications

FDA FEI Number

1000111640 528 3008311900 434 3004824601 413 3012251300 372 3012316249 351 3004905643 347 3014258441 303 3015005470 298 3016678950 298 3012841710 291 3017555752 291 1043214 272 3017264244 263 2311923 260 3002806913 260 3003238222 260 3003454229 260 3004373978 260 3007740591 260 3009684923 260 + More FDA FEI Numbers

Regulation

Us FDA 541 + More Regulations

FDA Registration Number

8043010 528 3008311900 434 3004824601 413 3012251300 372 3012316249 351 3004905643 347 3014258441 303 3015005470 298 3016678950 298 3012841710 291 3017555752 291 1043214 272 3017264244 263 2311923 260 3003238222 260 3003454229 260 3007740591 260 3009684923 260 3011539161 260 3012651177 260 + More FDA Registration Numbers

FDA K Number

K000581 1 K000609 1 K000740 1 K000816 1 K001288 1 K001317 1 K001349 1 K001608 1 K001718 1 K002109 1 K002411 1 K002488 1 K002827 1 K002908 1 K002910 1 K003010 1 K003272 1 K003520 1 K003707 1 K003748 1 + More FDA K Numbers

Massager, Therapeutic, Electric

FDA classification

FDA Class 1 ·Massager, Therapeutic, Electric

<1 …24 25 26 27 28 >

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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