PPA - BEUDAMED

BEUDAMED

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1,921 results · 23ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 2k FDA classification 249 + More Filters

Country

United States 2k Malaysia 23 United Kingdom 3 Australia 1 Canada 1 Thailand 1 + More Countries

Classification

FDA Class 1 2k + More Classifications

FDA FEI Number

1000122536 414 3007208013 363 3017539597 354 3008174888 335 3012494290 328 1048735 323 1831638 314 1000123180 311 3006236690 309 3002750084 304 3005182159 300 1000125183 298 1114298 296 3008624479 293 3006158025 287 3005182157 282 1417592 278 3009189893 278 1640981 275 3004107906 275 + More FDA FEI Numbers

Regulation

Us FDA 2k + More Regulations

FDA Registration Number

1528450 414 3007208013 363 3017539597 354 3008174888 335 3012494290 328 1048735 323 1831638 314 1123137 311 3006236690 309 1836161 304 3005182159 300 2028492 298 1114298 296 3008624479 293 3006158025 287 3005182157 282 1417592 278 3009189893 278 1640981 275 3004107906 275 + More FDA Registration Numbers

FDA K Number

K023046 1 K050063 1 K051409 1 K760027 1 K760031 1 K760032 1 K760278 1 K760485 1 K760487 1 K760496 1 K760602 1 K760623 1 K760838 1 K760908 1 K761000 1 K761001 1 K761062 1 K761138 1 K761170 1 K761174 1 + More FDA K Numbers

Methyl Orange

FDA classification

FDA Class 1 ·Methyl Orange

<1 …93 94 95 96 97 >

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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