MICROBIOLOGICS INC. - BEUDAMED

BEUDAMED

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21 results · 33ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 21 + More Filters

Country

United States 21 + More Countries

Classification

FDA Class 1 21 + More Classifications

FDA FEI Number

1924669 19 1119779 17 3003750284 16 2022807 15 3006224287 14 2150138 13 3002807578 13 3009547954 13 1210083 12 2242239 12 3006440892 12 3013160357 12 1000220444 11 1000354384 11 1050138 11 2916932 11 3002806955 11 3007808629 11 3008237827 11 3009307598 11 + More FDA FEI Numbers

Regulation

Us FDA 21 + More Regulations

FDA Registration Number

1924669 19 1119779 17 3003750284 16 2022807 15 8010096 14 2150138 13 3009547954 13 9610649 13 1210083 12 2242239 12 3006440892 12 3013160357 12 1050138 11 2016672 11 2916932 11 3009307598 11 3016741564 11 8010383 11 9611413 11 9615754 11 + More FDA Registration Numbers

C. ALBICANS SCREEN

FDA Class 1 ·Microbiology

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

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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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