Taiwan FDA registration b3d637135071fc70cb32c2875671fcf1
“GC” Dry Mouth Gel (Non-Sterile)
TW: “而至”口腔凝膠(未滅菌)
Taiwan·Risk Class 1·MD·GC CORPORATION FUJI OYAMA FACTORY·Registered Dec 12, 2018 – Dec 12, 2028ActiveRegistration details
- Analysis ID
- b3d637135071fc70cb32c2875671fcf1
- License Form
- Ministry of Health Medical Device Import No. 019919
- Customs Code
- DHA09401991903
Company information
- Manufacturer
- GC CORPORATION FUJI OYAMA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- GC TAIWAN DENTAL CORPORATION
Product details
- Intended Use
- Limit the first level identification range of liquid bandages (J.5090) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5090 Liquid bandages
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 12, 2018
- Expiry Date
- Dec 12, 2028
About this record
Access comprehensive regulatory information for “GC” Dry Mouth Gel (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b3d637135071fc70cb32c2875671fcf1 and manufactured by GC CORPORATION FUJI OYAMA FACTORY. The authorized representative in Taiwan is GC TAIWAN DENTAL CORPORATION.
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