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“GC” EXACLEAR - Taiwan Registration fc7e39c39e0e3a181769b4c2140a74b8

Access comprehensive regulatory information for “GC” EXACLEAR in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fc7e39c39e0e3a181769b4c2140a74b8 and manufactured by GC CORPORATION FUJI OYAMA FACTORY. 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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fc7e39c39e0e3a181769b4c2140a74b8
Registration Details
Taiwan FDA Registration: fc7e39c39e0e3a181769b4c2140a74b8
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Device Details

“GC” EXACLEAR
TW: “而至”艾哲透明印模材
Risk Class 2
MD

Registration Details

fc7e39c39e0e3a181769b4c2140a74b8

Ministry of Health Medical Device Import No. 034022

DHA05603402201

Company Information

Product Details

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

F Dental devices

F3660 impression material

Imported from abroad

Dates and Status

Nov 15, 2020

Nov 15, 2025