PMB - BEUDAMED

BEUDAMED

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2,161 results · 30ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 1 ×

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FDA 510(k) 2k FDA classification 146 + More Filters

Country

United States 2k Canada 69 Taiwan 38 China 34 Hong Kong 14 Australia 4 Germany 4 United Kingdom 4 Denmark 3 France 3 Indonesia 3 Netherlands 3 Honduras 2 Switzerland 2 Austria 1 Greece 1 Israel 1 Japan 1 Mexico 1 New Zealand 1 + More Countries

Classification

FDA Class 1 2k + More Classifications

FDA FEI Number

3012316249 1k 3926 1k 1417592 1k 3017264244 1k 3004824601 935 3013042114 909 1000143485 859 3004905643 852 3004727093 822 3016678950 804 3010394125 771 3015058854 755 3004034546 743 3004443928 743 3001657382 732 3007499787 732 3023189540 732 3003327839 727 3014421917 714 3009265647 712 + More FDA FEI Numbers

Regulation

Us FDA 2k + More Regulations

FDA Registration Number

3012316249 1k 8022890 1k 1417592 1k 3017264244 1k 3004824601 935 3013042114 909 1422443 859 3004905643 852 3004727093 822 3016678950 804 3010394125 771 3015058854 755 3004034546 743 3004443928 743 3001657382 732 3007499787 732 3023189540 732 9618009 727 3014421917 714 3009265647 712 + More FDA Registration Numbers

FDA K Number

Den110009 1 K000174 1 K000497 1 K000602 1 K000738 1 K001252 1 K001298 1 K001391 1 K001890 1 K001909 1 K002167 1 K002170 1 K002202 1 K002205 1 K002317 1 K002669 1 K002670 1 K002671 1 K002673 1 K002859 1 + More FDA K Numbers

Dispenser, Solid Medication

FDA classification

FDA Class 1 ·Dispenser, Solid Medication

<1 …105 106 107 108 109 >

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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