K130009 - BEUDAMED

BEUDAMED

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141 results · 42ms · Sources: EU EUDAMED, US FDA

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FDA Pre-Market Approval 102 FDA registration 27 FDA UDI 5 FDA classification 4 FDA 510(k) 3 + More Filters

Country

United States 127 Germany 5 Switzerland 4 China 2 Hong Kong 1 Singapore 1 South Korea 1 + More Countries

Classification

FDA Class 3 103 FDA Class 2 4 FDA Class 1 2 + More Classifications

FDA FEI Number

2011171 108 1721676 105 2648045 104 3002534070 104 3002807111 104 3002807314 104 1713910 103 2015691 103 3007063218 103 2025587 102 2182269 102 3002806434 102 3005334138 102 3007113487 102 3009380063 102 3009420598 102 3010421104 102 3010432890 102 3011894841 102 3012148004 102 + More FDA FEI Numbers

Regulation

Us FDA 141 + More Regulations

FDA Registration Number

2011171 108 1721676 105 2648045 104 3002807314 104 2015691 103 3007063218 103 3008500478 103 2025587 102 2135147 102 2182269 102 3005941719 102 3007113487 102 3009380063 102 3009420598 102 3010421104 102 3010432890 102 3011894841 102 3012148004 102 3012179728 102 3014918977 102 + More FDA Registration Numbers

FDA K Number

K000046 1 K000066 1 K000153 1 K000198 1 K000636 1 K000691 1 K001226 1 K001311 1 K001741 1 K001918 1 K001941 1 K001945 1 K002008 1 K002040 1 K002088 1 K002184 1 K002361 1 K002402 1 K002437 1 K002486 1 + More FDA K Numbers

Arthroscope

FDA classification

FDA Class 2 ·Arthroscope

<1 …4 5 6 7 8 >

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

BEUDAMED

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Imprint

BEUDAMED

Rationale
MDR Notified Bodies
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Tools

510(k) Predicate Finder
Product Code Directory
510(k) Review Times
21 CFR Regulations
NB Comparison

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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