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“Ivoclar Vivadent” IPS e.max CAD for KaVo ARCTICA - Taiwan Registration 6ebcbc477de9ab2a12abb70e2cf402be

Access comprehensive regulatory information for “Ivoclar Vivadent” IPS e.max CAD for KaVo ARCTICA in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6ebcbc477de9ab2a12abb70e2cf402be and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is MYWAY INTERNATIONAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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6ebcbc477de9ab2a12abb70e2cf402be
Registration Details
Taiwan FDA Registration: 6ebcbc477de9ab2a12abb70e2cf402be
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Device Details

“Ivoclar Vivadent” IPS e.max CAD for KaVo ARCTICA
TW: “義獲嘉偉瓦登特”阿堤卡齒雕機易美瓷塊
Risk Class 2
MD
Cancelled

Registration Details

6ebcbc477de9ab2a12abb70e2cf402be

Ministry of Health Medical Device Import No. 030350

DHA05603035001

Company Information

Liechtenstein

Product Details

F Dental devices

F6660 Dental porcelain powder

Imported from abroad

Dates and Status

Oct 17, 2017

Oct 17, 2022

Feb 27, 2018

Cancellation Information

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