CADWELL INDUSTRIES, INC. - BEUDAMED

BEUDAMED

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381 results · 126ms · Sources: EU EUDAMED, US FDA

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FDA UDI 320 FDA registration 32 Importer 15 FDA 510(k) 11 Authorized representative 2 Manufacturer 1 + More Filters

Country

United States 362 Germany 3 Denmark 2 Netherlands 2 Spain 2 Australia 1 Belgium 1 China 1 Czechia 1 Finland 1 Hungary 1 Italy 1 Lithuania 1 Poland 1 Slovenia 1 + More Countries

Manufacturer

Cadwell Industries, Inc. 16 The Magstim Company Limited 8 Ad Tech Medical Instrument Corp. 6 Braebon Medical Corporation 4 Digitimer Ltd 4 Dymedix Diagnostics, Inc. 3 Electro Cap Int.Inc. 3 Medoc Ltd 3 Cam Ntech Ltd 2 D. E. Hokanson, Inc. 2 Graphic Controls Acquisition Corp D.B.A Nissha Medical Technologies 2 Lumitex Medical Devices, Inc. 2 Neur Optics, Inc. 2 Nonin Medical, Inc. 2 S.L.P. Ltd. 2 Schiller Ag 2 Viasonix Ltd. 2 3 Cpm Company, Inc. 1 A.B. Dental Devices Ltd 1 A.R Guide In Medical Ltd. 1 + More Manufacturers

Competent Authority

Ministry Of Health, Welfare And Sports 3 Agencia Española De Medicamentos Y Productos Sanitarios 2 De/Ca304 Marktüberwachung Medizinprodukte Bayern 2 Danish Medicines Agency, Pharmacovigilance & Medical Devices 2 Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia: Medical Devices Division / Pharmaceutical Inspection Division – Medical Devices Unit 1 De/Ca32 Landesamt Für Soziales, Jugend Und Versorgung 1 Federal Agency For Medicines And Health Products / / Health Products Division 1 Finnish Medicines Agency, Supervision And Licences, Medical Device Unit 1 Ministry Of Health Directorate General Of Medical Devices And Pharmaceutical Services 1 Nemzeti Népegészségügyi és Gyógyszerészeti Központ 1 State Health Care Accreditation Agency Under The Ministry Of Health Of The Republic Of Lithuania 1 State Institute For Drug Control Medical Device Section 1 The Office For Registration Of Medicinal Products, Medical Devices And Biocidal Products 1 + More Competent Authorities

Classification

FDA Class 2 11 + More Classifications

FDA FEI Number

3020018 41 3002809369 11 1000139867 10 2080783 10 3002807720 10 3002807739 10 3010611950 10 3013501110 10 3016852448 10 2023374 9 3001687738 9 3006418479 9 3007611554 9 3007962724 9 3002716534 8 3003255845 8 3003851073 8 3004674371 8 1045254 7 3000126629 7 + More FDA FEI Numbers

Regulation

Us FDA 363 + More Regulations

Authorized Representative

C Epartner4 U 1 + More Authorized Representatives

FDA Registration Number

3020018 41 9612330 11 2080783 10 2184161 10 3010611950 10 3013501110 10 3016852448 10 8030229 10 9611252 10 2023374 9 3001687738 9 3006418479 9 3007611554 9 3007962724 9 1650946 8 3003851073 8 9612389 8 9613619 8 1045254 7 1063925 7 + More FDA Registration Numbers

Llins Service & Consulting GmbH

Authorized representative

🇩🇪 Germany·39 Manufacturers·556 Devices

<1 …16 17 18 19 20 >

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

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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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