CHROMA ATE INC. - BEUDAMED

BEUDAMED

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21 results · 110ms · Sources: EU EUDAMED, US FDA

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Device 11 Basic UDI-DI 4 FDA registration 2 Authorized representative 1 FDA UDI 1 Importer 1 Manufacturer 1 + More Filters

Country

Taiwan 18 Germany 1 Spain 1 United States 1 + More Countries

Manufacturer

Chroma Ate Inc. 16 Adstec Corporation 1 Aehealth Limited 1 Aivf Ltd. 1 Akisa (Hk) Co., Limited 1 American Comb Corp 1 Art Medical Ltd. 1 Arum Dentistry Co., Ltd. 1 Abrasive Technology Llc 1 Accelcare Products Corp. 1 Accu Bio Med Co., Ltd. 1 Ace Medical Technology Co., Ltd. 1 Acegreen Eco Material Technology Co. Ltd. 1 Acmex Bio Technology (Chongqing) Co., Ltd. 1 Acon Biotech (Hangzhou) Co., Ltd. 1 Acro Biotech Inc. 1 Adin Dental Implant Systems Ltd. 1 Aehealth Limited 1 Aeon Biotherapeutics Corp. 1 Aidite（Qinhuangdao）Technology Co.,Ltd. 1 + More Manufacturers

Competent Authority

De/Ca22 Bezirksregierung Münster 17 Agencia Española De Medicamentos Y Productos Sanitarios 1 + More Competent Authorities

Kind

Instrument 4 Professional Testing 4 Single Use 3 + More Kinds

Classification

Eu Ivd Class A 15 + More Classifications

FDA FEI Number

3003083993 2 + More FDA FEI Numbers

Regulation

Eu Ivdr 15 Us FDA 3 + More Regulations

Authorized Representative

Med Net Ec Rep Gmb H 16 + More Authorized Representatives

FDA Registration Number

3003083993 2 + More FDA Registration Numbers

Status

On The Market 11 + More Statuses

MedNet EC-REP GmbH

Authorized representative

🇩🇪 Germany·464 Manufacturers·5263 Devices

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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