“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.
Device Details
Registration Details
6ebcbc477de9ab2a12abb70e2cf402be
Ministry of Health Medical Device Import No. 030350
DHA05603035001
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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