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“Ivoclar Vivadent”Preformed Impression Tray (Non-Sterile)  - Taiwan Registration 41f8a4187badb040072a0aa3042dd556

Access comprehensive regulatory information for “Ivoclar Vivadent”Preformed Impression Tray (Non-Sterile)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 41f8a4187badb040072a0aa3042dd556 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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41f8a4187badb040072a0aa3042dd556
Registration Details
Taiwan FDA Registration: 41f8a4187badb040072a0aa3042dd556
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Device Details

“Ivoclar Vivadent”Preformed Impression Tray (Non-Sterile) 
TW: “義獲嘉偉瓦登特”成形印模牙托 (未滅菌) 
Risk Class 1
MD

Registration Details

41f8a4187badb040072a0aa3042dd556

Ministry of Health Medical Device Import Registration No. 009255

DHA08400925503

Company Information

Liechtenstein

Product Details

F Dental devices

F6880 Formed impression tray

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025

Aug 04, 2023