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“Ivoclar Vivadent” Callisto CPG - Taiwan Registration fe370bbab9fbb985dea1aef9a91760b7

Access comprehensive regulatory information for “Ivoclar Vivadent” Callisto CPG in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe370bbab9fbb985dea1aef9a91760b7 and manufactured by IVOCLAR VIVADENT, INC.. The authorized representative in Taiwan is BioLaden Consultant Corp..

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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fe370bbab9fbb985dea1aef9a91760b7
Registration Details
Taiwan FDA Registration: fe370bbab9fbb985dea1aef9a91760b7
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Device Details

“Ivoclar Vivadent” Callisto CPG
TW: “義獲嘉偉瓦登特”卡利朵牙科用基底合金
Risk Class 2
MD

Registration Details

fe370bbab9fbb985dea1aef9a91760b7

Ministry of Health Medical Device Import No. 031162

DHA05603116202

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F3060 Dentistry uses gold base alloys and precious metal alloys

Imported from abroad

Dates and Status

May 31, 2018

May 31, 2028