Interacoustics A/S - BEUDAMED

BEUDAMED

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341 results · 100ms · Sources: EU EUDAMED, US FDA

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FDA UDI 269 FDA registration 46 FDA 510(k) 25 Manufacturer 1 + More Filters

Country

United States 278 Denmark 63 + More Countries

Competent Authority

Danish Medicines Agency, Pharmacovigilance & Medical Devices 1 + More Competent Authorities

Classification

FDA Class 2 22 FDA Unclassified 3 + More Classifications

FDA FEI Number

3000254565 71 3002807554 25 3005581270 25 3011310592 25 2113281 16 3002504821 16 3008111228 16 3002809369 15 3008699634 15 3012118649 14 1316463 13 3003138182 13 3010608097 13 1000113738 12 2939 12 3000279201 12 3004046843 12 3006418479 12 3008881376 12 1000307595 10 + More FDA FEI Numbers

Regulation

Us FDA 340 + More Regulations

FDA Registration Number

9710051 71 3005581270 25 3011310592 25 9612197 25 2113281 16 3002504821 16 3008111228 16 3008699634 15 9612330 15 3012118649 14 1316463 13 3003138182 13 3010608097 13 1052723 12 3000279201 12 3004046843 12 3006418479 12 3008881376 12 8021990 12 1058264 10 + More FDA Registration Numbers

ECLIPSE (CABINET NAME), TEOAE25, EP15, OR THE COMBINATION OF SYSTEMS.

FDA Class 2 ·Ear, Nose, Throat

<1 …14 15 16 17 18 >

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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