Taiwan FDA registration b00fda2704b4fbae33972fcac34bae18
“GC” Coe-Pak
TW: “而至” 寇派克暫時性黏著劑
Registration details
- Analysis ID
- b00fda2704b4fbae33972fcac34bae18
- License Form
- Ministry of Health Medical Device Import No. 031002
- Customs Code
- DHA05603100206
Company information
- Manufacturer
- GC AMERICA INC.
- Manufacturer Country
- United States
- 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)
- F3275 Dental cement (Sminting)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 28, 2018
- Expiry Date
- Mar 28, 2028
About this record
Access comprehensive regulatory information for “GC” Coe-Pak in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b00fda2704b4fbae33972fcac34bae18 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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