MEDIATECH, INC. - BEUDAMED

BEUDAMED

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521 results · 68ms · Sources: EU EUDAMED, US FDA

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FDA registration 303 FDA UDI 63 FDA 510(k) 43 Importer 30 Authorized representative 25 Device 25 Basic UDI-DI 24 Manufacturer 6 Certificate 2 + More Filters

Country

China 231 Canada 113 United States 103 Netherlands 12 Germany 11 India 10 Ireland 10 Spain 5 France 4 Romania 4 Denmark 3 Taiwan 3 Belgium 2 Finland 2 Malta 2 South Korea 2 Czechia 1 Portugal 1 Sweden 1 + More Countries

Manufacturer

Meditech International Inc 37 Bio Tech Vision Care Pvt. Ltd. 9 Guangdong Biolight Meditech Co., Ltd 9 Edan Instruments,Inc. 7 Shenzhen Comen Medical Instruments Co.,Ltd. 7 Promisemed Hangzhou Meditech Co., Ltd. 5 Changsha Sinocare Inc. 4 Changzhou Major Medical Products Co.,Ltd 4 Intco Medical (Hk) Co., Ltd 4 Ivor Shaw Ltd Trading As Pennine Healthcare 4 Shanghai Chemtron Biotech Co., Ltd. 4 Shenzhen Mindray Bio Medical Electronics Co., Ltd. 4 Sun Tech Medical, Inc 4 Anhui Tiankang Medical Technology Co., Ltd. 3 Anrei Medical (Hz) Co., Ltd. 3 Atrion Medical Products, Inc. 3 Bio Protech Inc. 3 Beijing Choice Electronic Technology Co., Ltd. 3 Cu Medical Systems, Inc. 3 Curexo, Inc. 3 + More Manufacturers

Competent Authority

Federal Agency For Medicines And Health Products / / Health Products Division 40 Health Products Regulatory Authority, Medical Devices Department 19 Ministry Of Health, Welfare And Sports 17 Agencia Española De Medicamentos Y Productos Sanitarios 6 Agence Nationale De Sécurité Du Médicament Et Des Produits De Santé 4 National Agency For Medicines And Medical Devices Of Romania 4 De/Ca29 Regierungspräsidium Darmstadt Abteilung Arbeitsschutz Und Umwelt 3 Danish Medicines Agency, Pharmacovigilance & Medical Devices 3 De/Ca20, Bezirksregierung Düsseldorf Dezernat 24 2 Finnish Medicines Agency, Supervision And Licences, Medical Device Unit 2 Malta Medicines Authority 2 De/Ca05 Behorde Fur Justiz Und Verbraucherschutz 1 De/Ca09 Staatliches Gewerbeaufsichtsamt Hannover 1 De/Ca21 Bezirksregierung Köln Dezernat 24 1 De/Ca304 Marktüberwachung Medizinprodukte Bayern 1 De/Ca32 Landesamt Für Soziales, Jugend Und Versorgung 1 De/Ca70 Landesamt Für Umwelt Und Arbeitsschutz 1 Infarmed – National Authority Of Medicines And Health Products, I.P 1 State Institute For Drug Control Medical Device Section 1 Swedish Medical Products Agency 1 + More Competent Authorities

Kind

Active 19 Single Use 6 Sterile 6 Measuring Function 1 + More Kinds

Classification

Eu Md Class 2a 33 FDA Class 1 23 FDA Class 2 19 Eu Md Class 2b 12 Eu Md Class 1 4 + More Classifications

Notified Body

Gmed Sas 34 Dnv Product Assurance As 4 + More Notified Bodies

FDA FEI Number

3005440795 223 3010375065 69 3013221738 32 3002836339 29 3010512490 29 1048735 27 1000123180 24 1000122536 23 1114298 23 1318354 23 2022379 23 3002806725 23 3004107906 23 3005182157 23 3005182159 23 3005875593 23 3006158025 23 3006236690 23 3008496303 23 3008624479 23 + More FDA FEI Numbers

Regulation

Us FDA 409 Eu Mdd 34 Eu Mdr 15 + More Regulations

Authorized Representative

Obelis S.A. 38 Biotech Europe Meditech Inc Limited 10 Lotus Nl B.V. 4 Ar Experts B.V. 1 Cmc Medical Devices & Drugs Sl 1 Certification Experts 1 + More Authorized Representatives

FDA Registration Number

3005440795 223 3010375065 69 3013221738 32 1226230 29 3010512490 29 1048735 27 1123137 24 1114298 23 1318354 23 1528450 23 2022379 23 3004107906 23 3005182157 23 3005182159 23 3005875593 23 3006158025 23 3006236690 23 3008496303 23 3008624479 23 3014015490 23 + More FDA Registration Numbers

Certificate Type

Mdd Annex Ii (Excluding Section 4) 38 + More Certificate Types

Status

On The Market 24 No Longer On The Market 1 + More Statuses

SUNGO Europe B.V.

Authorized representative

🇳🇱 Netherlands·1571 Manufacturers·20390 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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