EAG - BEUDAMED

BEUDAMED

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2,161 results · 26ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 2k FDA classification 134 FDA Pre-Market Approval 21 + More Filters

Country

United States 2k Germany 53 United Kingdom 44 Denmark 41 Sweden 33 China 31 Japan 28 Canada 27 Netherlands 16 Austria 12 Switzerland 11 Israel 9 France 7 Italy 7 Australia 5 Egypt 5 Taiwan 5 Ireland 4 South Korea 4 South Africa 3 + More Countries

Classification

FDA Class 2 2k + More Classifications

FDA FEI Number

3018094310 980 3013557562 933 3011050570 920 1928237 756 3012494290 750 1045254 716 3002808268 681 3007475226 681 3010707607 681 3014342096 681 2020550 680 3003790304 669 1048735 664 3012636179 656 3003495548 648 2183744 644 1037007 643 3016678045 625 3002808001 544 3017636737 532 + More FDA FEI Numbers

Regulation

Us FDA 2k + More Regulations

FDA Registration Number

3018094310 980 3013557562 933 3011050570 920 1928237 756 3012494290 750 1045254 716 3010202439 681 3010707607 681 3014342096 681 9610617 681 2020550 680 3003790304 669 1048735 664 3012636179 656 9612501 648 2183744 644 1037007 643 3016678045 625 9611102 544 3017636737 532 + More FDA Registration Numbers

FDA K Number

Den020003 1 Den050007 1 Den070014 1 Den100025 1 Den130039 1 Den130046 1 Den150002 1 Den150056 1 Den160056 1 Den170009 1 Den170010 1 Den170023 1 Den170043 1 Den170044 1 Den170045 1 Den170075 1 Den170078 1 Den180005 1 Den180026 1 Den190055 1 + More FDA K Numbers

Masker, Tinnitus

FDA classification

FDA Class 2 ·Masker, Tinnitus

<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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