CHQ - BEUDAMED

BEUDAMED

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581 results · 39ms · Sources: EU EUDAMED, US FDA

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FDA classification 581 + More Filters

Country

United States 581 + More Countries

Classification

FDA Class 1 316 FDA Class 2 233 FDA Class 3 18 FDA Not Classified 12 + More Classifications

FDA FEI Number

2432235 118 3002806559 116 3006198300 110 3015550354 103 2517506 91 3005333358 78 1832216 75 3004493545 71 1000136573 69 1000206808 65 3022178699 65 1181121 63 2250051 63 3003795116 63 1827821 61 3002809144 61 2050012 59 3003741796 58 3002642396 55 1036362 54 + More FDA FEI Numbers

Regulation

Us FDA 581 + More Regulations

FDA Registration Number

2432235 118 9610126 116 3006198300 110 3015550354 103 2517506 91 3005333358 78 1832216 75 3004493545 71 1319681 69 3022178699 65 9680746 65 1181121 63 2250051 63 3003795116 63 1827821 61 3002809144 61 2050012 59 3003741796 58 3002642396 55 1036362 54 + More FDA Registration Numbers

FDA K Number

Den000010 1 Den030001 1 Den040002 1 Den040012 1 Den080007 1 Den130002 1 Den130031 1 Den130042 1 Den140016 1 Den140038 1 Den150035 1 Den150057 1 Den170019 1 Den170043 1 Den170088 1 Den180004 1 Den180007 1 Den180028 1 Den180056 1 Den180058 1 + More FDA K Numbers

Data Acquisition Software

FDA classification

FDA Class 2 ·Data Acquisition Software

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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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