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BEUDAMED

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521 results · 46ms · Sources: EU EUDAMED, US FDA

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FDA Pre-Market Approval 521 + More Filters

Country

United States 521 + More Countries

Classification

FDA Class 3 461 FDA Class 2 57 + More Classifications

FDA FEI Number

2011068 254 3003347293 250 3003407669 249 3013840437 249 3015373820 247 3026391021 247 3030390308 247 3033486016 247 3037006441 247 1000118068 246 3006123332 246 3007093114 246 3009882464 246 3002807108 245 3003672980 245 3003707320 245 3004362706 245 3004423487 245 3005113652 245 3005975625 245 + More FDA FEI Numbers

Regulation

Us FDA 521 + More Regulations

FDA Registration Number

2011068 254 9710154 250 2135225 249 3013840437 249 3015373820 247 3026391021 247 3030390308 247 3033486016 247 3037006441 247 1000118068 246 3006123332 246 3007093114 246 3009882464 246 3002807108 245 3003672980 245 3003707320 245 3004362706 245 3004423487 245 3005113652 245 3005975625 245 + More FDA Registration Numbers

Immunocytochemistry Assay, P16/Ki-67

FDA Pre-Market Approval

FDA Class 3 ·CINtec PLUS Cytology

<1 …23 24 25 26 27 >

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

BEUDAMED

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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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