QMA - BEUDAMED

BEUDAMED

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1,021 results · 24ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 1k FDA classification 1 + More Filters

Country

United States 1k Taiwan 4 Hong Kong 1 Netherlands 1 + More Countries

Classification

FDA Class 1 1k + More Classifications

FDA FEI Number

3012494290 339 3007208013 336 3002750084 313 1417592 277 2432235 252 3002806559 247 3006198300 244 3013557562 240 3012421607 228 3003418325 224 1043214 221 3001236905 221 3005333358 221 1827821 220 3015550354 219 1000136573 211 1220477 211 1832216 197 1000112877 190 2250051 190 + More FDA FEI Numbers

Regulation

Us FDA 1k + More Regulations

FDA Registration Number

3012494290 339 3007208013 336 1836161 313 1417592 277 2432235 252 9610126 247 3006198300 244 3013557562 240 3012421607 228 3003418325 225 1043214 221 1423537 221 3005333358 221 1827821 220 3015550354 219 1220477 211 1319681 211 1832216 197 1054241 190 2250051 190 + More FDA Registration Numbers

FDA K Number

K770120 1 K821177 1 K830705 1 K842461 1 K992995 1 + More FDA K Numbers

OXYHEMOGLOBIN CONTROL FOR CO-OXIMETRY

FDA Class 1 ·Clinical Chemistry

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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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