LSA - BEUDAMED

BEUDAMED

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921 results · 26ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 397 FDA classification 345 FDA Pre-Market Approval 179 + More Filters

Country

United States 824 Canada 28 France 27 China 16 Saudi Arabia 11 Spain 5 South Korea 2 Finland 1 Germany 1 India 1 Mexico 1 Norway 1 Sweden 1 Switzerland 1 United Kingdom 1 + More Countries

Classification

FDA Class 2 921 + More Classifications

FDA FEI Number

1047843 190 1450662 179 3000206435 176 2011171 173 1000138054 171 1000306431 169 1721676 166 3003076831 166 2124215 165 3000126629 158 3016678045 157 1018233 155 1928237 154 2528981 150 3006082230 150 3009617712 150 3009077524 148 1417592 144 3010703925 139 3010605677 138 + More FDA FEI Numbers

Regulation

Us FDA 921 + More Regulations

FDA Registration Number

1047843 190 1450662 179 2030624 176 2011171 173 1319639 171 2029275 169 1721676 166 2032112 166 2124215 165 3000126629 158 3016678045 157 1018233 155 1928237 154 2528981 150 3006082230 150 3009617712 150 3009077524 148 1417592 144 3010703925 139 3010605677 138 + More FDA Registration Numbers

FDA K Number

Den020001 1 Den020003 1 Den040004 1 Den040007 1 Den040012 1 Den050002 1 Den050004 1 Den060001 1 Den060007 1 Den070002 1 Den070003 1 Den070009 1 Den070013 1 Den070014 1 Den080009 1 Den090002 1 Den090004 1 Den100025 1 Den110002 1 Den110011 1 + More FDA K Numbers

Human Lyophilized Dura Mater

FDA classification

FDA Class 2 ·Human Lyophilized Dura Mater

<1 …43 44 45 46 47 >

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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