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“Ivoclar Vivadent” Vivaglass - Taiwan Registration 7609a19056f0f3f9a0babd04fb7958b2

Access comprehensive regulatory information for “Ivoclar Vivadent” Vivaglass in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7609a19056f0f3f9a0babd04fb7958b2 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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7609a19056f0f3f9a0babd04fb7958b2
Registration Details
Taiwan FDA Registration: 7609a19056f0f3f9a0babd04fb7958b2
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Device Details

“Ivoclar Vivadent” Vivaglass
TW: “義獲嘉偉瓦登特”偉瓦玻璃離子黏合劑
Risk Class 2
MD

Registration Details

7609a19056f0f3f9a0babd04fb7958b2

Ministry of Health Medical Device Import No. 031083

DHA05603108306

Company Information

Liechtenstein

Product Details

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

F Dental devices

F3275 Dental cement (Sminting)

Imported from abroad

Dates and Status

May 16, 2018

May 16, 2023