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“Ivoclar Vivadent” VivaSens - Taiwan Registration 571bb5e0da3e086ff2fb9e286225b6ef

Access comprehensive regulatory information for “Ivoclar Vivadent” VivaSens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 571bb5e0da3e086ff2fb9e286225b6ef 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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571bb5e0da3e086ff2fb9e286225b6ef
Registration Details
Taiwan FDA Registration: 571bb5e0da3e086ff2fb9e286225b6ef
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Device Details

“Ivoclar Vivadent” VivaSens
TW: “義獲嘉偉瓦登特”偉瓦先施牙齒保護劑
Risk Class 2
MD

Registration Details

571bb5e0da3e086ff2fb9e286225b6ef

Ministry of Health Medical Device Import No. 031253

DHA05603125305

Company Information

Liechtenstein

Product Details

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

F Dental devices

F3260 Cave coating

Imported from abroad

Dates and Status

Jun 22, 2018

Jun 22, 2028