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BEUDAMED

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

Filters Classification: FDA Class 2 ×

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FDA 510(k) 60 FDA Pre-Market Approval 1 + More Filters

Country

United States 34 Netherlands 12 Germany 11 Greece 2 Finland 1 Sweden 1 + More Countries

Classification

FDA Class 2 61 + More Classifications

FDA FEI Number

3018094310 26 3001236277 22 1047843 20 3009973505 20 3016438694 20 1720929 19 3002808269 19 3002907620 19 1828464 18 3000126629 18 3003128516 18 3005061536 18 1000306340 17 1043653 17 1818910 17 1825034 17 2183301 17 3000209794 17 3002468371 17 3003477135 17 + More FDA FEI Numbers

Regulation

Us FDA 61 + More Regulations

FDA Registration Number

3018094310 26 1649518 22 1047843 20 3009973505 20 3016438694 20 1720929 19 3002907620 19 8043792 19 1226544 18 1828464 18 3000126629 18 3005061536 18 1043653 17 1818910 17 1825034 17 1834331 17 2133772 17 2183301 17 3003477135 17 3003935342 17 + More FDA Registration Numbers

STOCKERT NEURO N50, MODEL12267

FDA Class 2 ·Neurology

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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