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“Ivoclar Vivadent” Telio Inlay/Onlay - Taiwan Registration b109208b69b9e28310c664ac6579faca

Access comprehensive regulatory information for “Ivoclar Vivadent” Telio Inlay/Onlay in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b109208b69b9e28310c664ac6579faca and manufactured by IVOCLAR VIVADENT AG. 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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b109208b69b9e28310c664ac6579faca
Registration Details
Taiwan FDA Registration: b109208b69b9e28310c664ac6579faca
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Device Details

“Ivoclar Vivadent” Telio Inlay/Onlay
TW: “義獲嘉偉瓦登特”特利歐牙科嵌體材料
Risk Class 2
MD

Registration Details

b109208b69b9e28310c664ac6579faca

Ministry of Health Medical Device Import No. 034723

DHA05603472305

Company Information

Liechtenstein

Product Details

Details are as detailed as approved Chinese instructions

F Dental devices

F3770 Temporary crown and bridge resin

Imported from abroad

Dates and Status

Jul 24, 2021

Jul 24, 2026