K221816 - BEUDAMED

BEUDAMED

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1,381 results · 42ms · Sources: EU EUDAMED, US FDA

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FDA 510(k) 1k FDA Pre-Market Approval 169 FDA registration 13 FDA classification 9 FDA UDI 3 + More Filters

Country

United States 1k China 45 United Kingdom 45 Canada 31 Taiwan 16 Ireland 8 New Zealand 8 France 6 Switzerland 6 Germany 4 Iceland 4 Israel 4 Belgium 3 Japan 3 Malaysia 3 Netherlands 3 Spain 2 Sweden 2 Costa Rica 1 Denmark 1 + More Countries

Classification

FDA Unclassified 1k FDA Class 2 170 FDA Class 3 168 FDA Class 1 4 + More Classifications

FDA FEI Number

1000148471 1k 3003418325 1k 1000306431 1k 1220477 1k 1000136478 1k 1047843 1k 2024024 1k 1450662 1k 2245304 1k 3001236277 1k 3002808269 1k 3012448339 1k 3002516348 1k 3004170064 1k 3005920706 1k 3007321028 1k 1018470 1k 1048735 1k 2183744 1k 2246552 1k + More FDA FEI Numbers

Regulation

Us FDA 1k + More Regulations

FDA Registration Number

1221816 1k 3003418325 1k 1220477 1k 2029275 1k 1047843 1k 2024024 1k 1225991 1k 1319660 1k 1450662 1k 1649518 1k 2245304 1k 3012448339 1k 8043792 1k 3004170064 1k 3005920706 1k 3007321028 1k 1018470 1k 1048735 1k 2183744 1k 2246552 1k + More FDA Registration Numbers

FDA K Number

K000048 1 K000051 1 K000054 1 K000144 1 K000253 1 K000396 1 K000438 1 K000456 1 K000487 1 K000747 1 K000865 1 K000870 1 K000947 1 K001023 1 K001055 1 K001117 1 K001474 1 K001519 1 K001521 1 K001731 1 + More FDA K Numbers

Syringe, Piston

FDA classification

FDA Class 2 ·Syringe, Piston

<1 …66 67 68 69 70 >

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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