Taiwan FDA registration fc7e39c39e0e3a181769b4c2140a74b8
“GC” EXACLEAR
TW: “而至”艾哲透明印模材
Taiwan·Risk Class 2·MD·GC CORPORATION FUJI OYAMA FACTORY·Registered Nov 15, 2020 – Nov 15, 2025ExpiredRegistration details
- Analysis ID
- fc7e39c39e0e3a181769b4c2140a74b8
- License Form
- Ministry of Health Medical Device Import No. 034022
- Customs Code
- DHA05603402201
Company information
- Manufacturer
- GC CORPORATION FUJI OYAMA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- GC TAIWAN DENTAL CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3660 impression material
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 15, 2020
- Expiry Date
- Nov 15, 2025
About this record
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.
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