DENT ZAR, INC. - BEUDAMED

BEUDAMED

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121 results · 92ms · Sources: EU EUDAMED, US FDA

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FDA UDI 86 FDA registration 22 FDA 510(k) 12 Authorized representative 1 + More Filters

Country

United States 120 Belgium 1 + More Countries

Manufacturer

Jade Scientific Inc. Dba American Scientific Products, Chem Pure Chemicals 1 Minaris Medical Co., Ltd. 1 3 Nt Medical 1 A Mi Global Co., Ltd. 1 A Spine Asia Co., Ltd. 1 Agd Biomedicals Pvt. Ltd 1 Ami Inc. 1 Aneuvo 1 Anjir Talaee 1 Asep Healthcare Ltd 1 Aspivix Sa 1 Austar Hearing Science & Technology (Xiamen) Co., Ltd. 1 Axg Industries Sdn Bhd 1 Azure Vault Ltd 1 Aadi Med Private Limited (Formerly Known As Shiva Products) 1 Abdos Labtech Private Limited 1 Acro Biotech Inc. 1 Admetec Solutions Ltd 1 Advance Dx, Inc. 1 Advanced Med Tech Solutions Private Limited 1 + More Manufacturers

Competent Authority

Federal Agency For Medicines And Health Products / / Health Products Division 1 + More Competent Authorities

Classification

FDA Class 2 12 + More Classifications

FDA FEI Number

2027375 34 1000118628 12 1000272892 12 1215305 12 1410097 12 1413475 12 1420052 12 1420089 12 1450653 12 1718476 12 1718912 12 2018957 12 2020467 12 2020493 12 2022039 12 2023950 12 2024312 12 2110898 12 2126683 12 3002718942 12 + More FDA FEI Numbers

Regulation

Us FDA 120 + More Regulations

FDA Registration Number

2027375 34 1000118628 12 1000272892 12 1215305 12 1410097 12 1413475 12 1420052 12 1420089 12 1424442 12 1450653 12 1718476 12 1718912 12 2018957 12 2020467 12 2020493 12 2022039 12 2023950 12 2024312 12 2024980 12 2110898 12 + More FDA Registration Numbers

Obelis s.a.

Authorized representative

🇧🇪 Belgium·546 Manufacturers·18515 Devices

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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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