BODYSTAT LTD - BEUDAMED

BEUDAMED

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21 results · 70ms · Sources: EU EUDAMED, US FDA

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FDA 510(k) 8 FDA UDI 6 FDA registration 5 Authorized representative 1 Importer 1 + More Filters

Country

United States 6 Isle Of Man 5 Brazil 4 United Kingdom 4 Italy 1 Slovenia 1 + More Countries

Manufacturer

Bodystat Limited 2 A Dec, Inc. 1 Acorda Therapeutics, Inc. 1 Acro Biotech Inc. 1 Alfresa Pharma Corporation 1 Anumana, Inc. 1 Cvaid Ltd. 1 Carbon Medical Technologies, Inc. 1 Co Ag Medical Llc 1 Coll Plant Ltd. 1 Fusmobile Israel Ltd 1 Glance Optical Pty Ltd 1 Genea Biomedx Pty Ltd 1 Globalcare Medical Technology Co., Ltd. 1 Hemostasis Llc 1 Lexion Medical Llc 1 Lorne Laboratories Ltd 1 Meridian Bioscience Israel Ltd. 1 Mycardium Ai Ltd 1 Oasis Medical, Inc. 1 + More Manufacturers

Competent Authority

Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia: Medical Devices Division / Pharmaceutical Inspection Division – Medical Devices Unit 1 Ministry Of Health Directorate General Of Medical Devices And Pharmaceutical Services 1 + More Competent Authorities

Classification

FDA Class 2 8 + More Classifications

FDA FEI Number

3006948217 12 1000029611 8 1000419277 8 3002684743 8 3003695829 8 3004782476 8 3005699942 8 3008240972 8 1000121041 7 1450057 7 3001058906 7 3003074886 7 3003193933 7 3003493780 7 3003587684 7 3003703880 7 3003741676 7 3004072282 7 3004485927 7 3004835896 7 + More FDA FEI Numbers

Regulation

Us FDA 19 + More Regulations

FDA Registration Number

3006948217 12 1122544 8 3002684743 8 3003695829 8 3004782476 8 3005699942 8 3008240972 8 9680010 8 1222304 7 1450057 7 2032852 7 3003074886 7 3003193933 7 3003587684 7 3003703880 7 3003741676 7 3004485927 7 3004835896 7 3005374248 7 3005707783 7 + More FDA Registration Numbers

Donawa Lifescience Consulting Srl

Authorized representative

🇮🇹 Italy·31 Manufacturers·15 Devices

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

BEUDAMED

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Imprint

BEUDAMED

Rationale
MDR Notified Bodies
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Tools

510(k) Predicate Finder
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510(k) Review Times
21 CFR Regulations
NB Comparison

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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