JUVORA LIMITED - BEUDAMED

BEUDAMED

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61 results · 60ms · Sources: EU EUDAMED, US FDA

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FDA UDI 42 Device 13 Authorized representative 2 Manufacturer 2 Basic UDI-DI 1 Certificate 1 + More Filters

Country

United States 42 Ireland 1 Netherlands 1 + More Countries

Manufacturer

Juvora Limited 17 A M Systems 1 Active Life Scientific, Inc. 1 Azena Medical, Llc 1 Adtec Healthcare Limited 1 Advanced Mechanical Technology, Inc. 1 Advantice Health Llc 1 Air Strip Technologies, Inc. 1 Ambulatory Monitoring, Inc. 1 Ambutech Inc. 1 Arbor Vita Corporation 1 Aretech, Llc 1 Attomarker Ltd 1 Awareness Technology, Inc. 1 Bonw Rx Ltd 1 Bxt Accelyon Limited 1 Belluscura Llc 1 Bernell Corporation 1 Bio Legend Inc 1 Bionostics 1 + More Manufacturers

Competent Authority

Health Products Regulatory Authority, Medical Devices Department 18 Ministry Of Health, Welfare And Sports 1 + More Competent Authorities

Kind

Implantable 1 + More Kinds

Classification

Eu Md Class 2a 14 + More Classifications

Notified Body

Sgs Belgium Nv 2 + More Notified Bodies

Regulation

Us FDA 42 Eu Mdr 14 + More Regulations

Authorized Representative

Med Envoy Global Bv 17 Psephos Limited 17 + More Authorized Representatives

Certificate Type

Mdr Qms 2 + More Certificate Types

Status

On The Market 13 + More Statuses

MedEnvoy Global BV

Authorized representative

🇳🇱 Netherlands·143 Manufacturers·2306 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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