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BEUDAMED

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441 results · 22ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 289 FDA Pre-Market Approval 147 FDA classification 5 + More Filters

Country

United States 405 Israel 13 Ireland 8 New Zealand 4 China 2 Japan 2 South Korea 2 Argentina 1 Canada 1 France 1 Germany 1 Netherlands 1 + More Countries

Classification

FDA Class 2 441 + More Classifications

FDA FEI Number

1043214 217 1000112877 206 1000112968 206 3018094310 147 1000114111 137 3007734888 116 3003190524 110 3003513129 108 3016860442 108 1000208608 104 3008729547 104 2080225 103 2027062 102 3006469671 101 3006791146 100 1000604079 95 3000210616 95 3002806988 95 3004050971 95 3010838917 95 + More FDA FEI Numbers

Regulation

Us FDA 441 + More Regulations

FDA Registration Number

1043214 217 1054241 206 1055236 206 3018094310 147 1054713 137 3007734888 116 9617277 109 3016860442 108 9710602 107 1057358 104 3008729547 104 2080225 103 2027062 102 3006791146 101 9613793 101 1000604079 95 2085602 95 3004050971 95 3010838917 95 3021559257 95 + More FDA Registration Numbers

FDA K Number

K000410 1 K002355 1 K003335 1 K012229 1 K020219 1 K020966 1 K033040 1 K060461 1 K070377 1 K072157 1 K090697 1 K101804 1 K102227 1 K120642 1 K120937 1 K121625 1 K122267 1 K123309 1 K173516 1 K191425 1 + More FDA K Numbers

Warmer, Infant Radiant

FDA classification

FDA Class 2 ·Warmer, Infant Radiant

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

BEUDAMED

A better medical device search engine by OpenRegulatory.

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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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