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“GC” Coe& Kooliner Denture Relining Material - Taiwan Registration 6435883b4fc81bc259ab506cf702b57b

Access comprehensive regulatory information for “GC” Coe& Kooliner Denture Relining Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6435883b4fc81bc259ab506cf702b57b and manufactured by GC AMERICA INC.. The authorized representative in Taiwan is GC TAIWAN DENTAL 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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6435883b4fc81bc259ab506cf702b57b
Registration Details
Taiwan FDA Registration: 6435883b4fc81bc259ab506cf702b57b
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Device Details

“GC” Coe& Kooliner Denture Relining Material
TW: “而至”寇怡庫萊義齒底墊材料
Risk Class 2
MD

Registration Details

6435883b4fc81bc259ab506cf702b57b

Ministry of Health Medical Device Import No. 031073

DHA05603107303

Company Information

United States

Product Details

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

F Dental devices

F3760 Denture re-liner re-reinding or replacement underlay resin

Imported from abroad

Dates and Status

May 11, 2018

May 11, 2028