K024022 - BEUDAMED

BEUDAMED

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1,401 results · 42ms · Sources: EU EUDAMED, US FDA

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FDA 510(k) 1k FDA registration 24 FDA classification 13 FDA UDI 6 + More Filters

Country

United States 1k United Kingdom 16 Israel 13 Switzerland 11 China 10 Canada 8 Germany 7 Taiwan 7 Australia 5 Italy 4 Costa Rica 3 France 2 Greece 1 Japan 1 Lithuania 1 New Zealand 1 Norway 1 Singapore 1 South Africa 1 Spain 1 + More Countries

Classification

FDA Class 2 1k FDA Class 1 197 + More Classifications

FDA FEI Number

2024022 1k 1000160458 1k 3013298431 1k 1921846 1k 3001236905 1k 3005601686 1k 3003076831 1k 3013557562 1k 3008002452 1k 3012494290 1k 1928237 1k 1220908 1k 2011171 1k 1000512168 1k 3018094310 1k 1000306431 1k 1219343 997 3001451571 997 3003327833 997 3002806934 992 + More FDA FEI Numbers

Regulation

Us FDA 1k + More Regulations

FDA Registration Number

2024022 1k 2029015 1k 3013298431 1k 1423537 1k 1921846 1k 9680741 1k 2032112 1k 3013557562 1k 1423507 1k 3012494290 1k 1928237 1k 1220908 1k 2011171 1k 1061124 1k 3018094310 1k 2029275 1k 1219343 997 1320894 997 9617787 997 9612030 992 + More FDA Registration Numbers

FDA K Number

K000209 1 K000246 1 K000265 1 K000266 1 K000328 1 K000821 1 K000842 1 K001052 1 K001629 1 K001643 1 K001828 1 K001829 1 K001833 1 K002051 1 K002126 1 K002211 1 K002380 1 K002444 1 K002608 1 K002679 1 + More FDA K Numbers

Garment, Protective, For Incontinence

FDA classification

FDA Class 1 ·Garment, Protective, For Incontinence

<1 …67 68 69 70 71 >

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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