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“Ivoclar Vivadent” Telio Temporary Restorative Material - Taiwan Registration 998daaee92f99ac17cdb91f191f2b56e

Access comprehensive regulatory information for “Ivoclar Vivadent” Telio Temporary Restorative Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 998daaee92f99ac17cdb91f191f2b56e 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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998daaee92f99ac17cdb91f191f2b56e
Registration Details
Taiwan FDA Registration: 998daaee92f99ac17cdb91f191f2b56e
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Device Details

“Ivoclar Vivadent” Telio Temporary Restorative Material
TW: “義獲嘉偉瓦登特”特利歐牙科用暫時性修復材料
Risk Class 2
MD

Registration Details

998daaee92f99ac17cdb91f191f2b56e

Ministry of Health Medical Device Import No. 034945

DHA05603494500

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

Sep 12, 2021

Sep 12, 2026