DENTALMAX CO.,LTD - BEUDAMED

BEUDAMED

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2,541 results · 105ms · Sources: EU EUDAMED, US FDA

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FDA UDI 3k FDA 510(k) 3 FDA registration 3 Authorized representative 2 Basic UDI-DI 1 Certificate 1 Device 1 Manufacturer 1 + More Filters

Country

United States 3k South Korea 10 Netherlands 2 + More Countries

Manufacturer

Dentalmax Co., Ltd 5 Ampall 2 Curexo, Inc. 2 Chiaro Technology Limited 2 Clari Pi Inc. 2 Cowellmedi Co., Ltd. 2 Dio Corporation 2 Dms Co., Ltd. 2 Dream Con Co., Ltd. 2 E Wha Meditech Inc. 2 Gonimed Co.,Ltd 2 Gyrozen 2 Hexar Humancare Co.,Ltd 2 Huvexel Co., Ltd. 2 Jmbiotech 2 Kims Med Co., Ltd. 2 Korea Vaccine Co., Ltd. 2 Medifive 2 Mcube Technology Co., Ltd 2 Medisarang Co.,Ltd 2 + More Manufacturers

Competent Authority

Ministry Of Health, Welfare And Sports 6 + More Competent Authorities

Kind

Single Use 1 + More Kinds

Classification

FDA Class 2 3 Eu Md Class 2a 2 + More Classifications

Notified Body

Udem Uluslararasi Belgelendirme Denetim Egitim Merkezi San. Ve Tic. A.ş. 4 + More Notified Bodies

FDA FEI Number

1000118628 3 1000120733 3 1000269600 3 1000426619 3 1219645 3 1316092 3 1410097 3 1420052 3 1420089 3 1718912 3 2018957 3 2020493 3 2023129 3 2023817 3 2082832 3 2244842 3 2433919 3 2523320 3 2647456 3 2916735 3 + More FDA FEI Numbers

Regulation

Us FDA 3k Eu Mdd 2 + More Regulations

Authorized Representative

Ar Experts B.V. 4 Certification Experts 4 + More Authorized Representatives

FDA Registration Number

1000118628 3 1000426619 3 1000625496 3 1064583 3 1064812 3 1219645 3 1222802 3 1316092 3 1410097 3 1420052 3 1420089 3 1718912 3 1725006 3 2018957 3 2020493 3 2023129 3 2023817 3 2082832 3 2244842 3 2424472 3 + More FDA Registration Numbers

Certificate Type

Mdd Annex V 4 + More Certificate Types

Status

On The Market 1 + More Statuses

AR Experts B.V.

Authorized representative

🇳🇱 Netherlands·65 Manufacturers·3355 Devices

<1 …124 125 126 127 128 >

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

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EU MDR

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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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