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“Dual Core” Dual-cured core build-up composite - Taiwan Registration 3b8fa7829a3a15423434cb1415dd9fe0

Access comprehensive regulatory information for “Dual Core” Dual-cured core build-up composite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3b8fa7829a3a15423434cb1415dd9fe0 and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT CORPORATION.

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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3b8fa7829a3a15423434cb1415dd9fe0
Registration Details
Taiwan FDA Registration: 3b8fa7829a3a15423434cb1415dd9fe0
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Device Details

“Dual Core” Dual-cured core build-up composite
TW: “帝卡”雙凝冠心建築樹脂
Risk Class 2
MD

Registration Details

3b8fa7829a3a15423434cb1415dd9fe0

Ministry of Health Medical Device Import No. 029620

DHA05602962001

Company Information

Korea, Republic of

Product Details

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

F Dental devices

F3690 Resin tusk wood

Imported from abroad

Dates and Status

Mar 31, 2017

Mar 31, 2027