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BEUDAMED

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441 results · 23ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 438 FDA classification 3 + More Filters

Country

United States 398 Malaysia 16 Ireland 8 Iran 5 United Kingdom 5 China 4 Canada 3 Argentina 1 Australia 1 + More Countries

Classification

FDA Class 1 441 + More Classifications

FDA FEI Number

3002806559 132 3015550354 129 2432235 128 3004493545 123 3006198300 123 1000136573 122 1616487 122 1827821 122 2050012 122 2517506 122 1000206808 121 2050010 121 3005333358 121 1417592 120 1832216 120 3002806560 120 3003795116 120 1000122044 119 1000135102 119 1181121 118 + More FDA FEI Numbers

Regulation

Us FDA 441 + More Regulations

FDA Registration Number

9610126 132 3015550354 129 2432235 128 3004493545 123 3006198300 123 1319681 122 1616487 122 1827821 122 2050012 122 2517506 122 2050010 121 3005333358 121 1417592 120 1832216 120 3003795116 120 9610529 120 9680746 120 2085064 119 2247288 119 3002809144 119 + More FDA Registration Numbers

FDA K Number

K003012 1 K003912 1 K013095 1 K022312 1 K030015 1 K041643 1 K072141 1 K100263 1 K760030 1 K760634 1 K760990 1 K761238 1 K761239 1 K770456 1 K770558 1 K770820 1 K771477 1 K771835 1 K771848 1 K772156 1 + More FDA K Numbers

FOLLICLE STIMULATING HORMONE-EIA-XT

FDA Class 1 ·Clinical Chemistry

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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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