K021924 - BEUDAMED

BEUDAMED

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1,641 results · 41ms · Sources: EU EUDAMED, US FDA

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FDA 510(k) 2k FDA registration 57 FDA classification 23 FDA Pre-Market Approval 3 FDA UDI 2 + More Filters

Country

United States 2k United Kingdom 84 Canada 11 Spain 7 Finland 5 Thailand 5 France 4 Japan 3 Taiwan 3 China 2 Denmark 2 Italy 2 Malaysia 2 New Zealand 2 Australia 1 Belgium 1 Czechia 1 Germany 1 Indonesia 1 Ireland 1 + More Countries

Classification

FDA Class 1 1k FDA Class 2 558 + More Classifications

FDA FEI Number

3002485711 2k 3007118747 2k 2432235 1k 3015550354 1k 3022178699 1k 2122870 1k 3002806944 1k 3006198300 1k 1000136573 1k 3002806559 1k 3007111389 1k 2250051 1k 3011989923 1k 2967 1k 3005529799 1k 1219913 1k 3000308930 1k 3002642396 1k 3012963943 1k 3002809144 1k + More FDA FEI Numbers

Regulation

Us FDA 2k + More Regulations

FDA Registration Number

8021924 2k 3007118747 2k 2432235 1k 3015550354 1k 3022178699 1k 2122870 1k 3002806944 1k 3006198300 1k 1319681 1k 9610126 1k 3007111389 1k 2250051 1k 3011989923 1k 8031673 1k 3005529799 1k 1219913 1k 3000308930 1k 3002642396 1k 3012963943 1k 3002809144 1k + More FDA Registration Numbers

FDA K Number

K000042 1 K000043 1 K000056 1 K000138 1 K000139 1 K000143 1 K000145 1 K000178 1 K000179 1 K000223 1 K000226 1 K000230 1 K000231 1 K000295 1 K000318 1 K000323 1 K000329 1 K000330 1 K000421 1 K000471 1 + More FDA K Numbers

Polymer Patient Examination Glove

FDA classification

FDA Class 1 ·Polymer Patient Examination Glove

<1 …79 80 81 82 83 >

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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