Taiwan FDA registration f0878a3c2e155e173b744817aff7ffb7
“Geistlich” Fibro-Gide Collagen Matrix
TW: “蓋氏”法博吉膠原蛋白基質
Taiwan·Risk Class 2·MD·GEISTLICH PHARMA AG·Registered Oct 29, 2020 – Oct 29, 2025ExpiredRegistration details
- Analysis ID
- f0878a3c2e155e173b744817aff7ffb7
- License Form
- Ministry of Health Medical Device Import No. 034009
- Customs Code
- DHA05603400909
Company information
- Manufacturer
- GEISTLICH PHARMA AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- EMERGO TAIWAN LIMITED
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)
- F3930 Alveolar Restoration Materials
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 29, 2020
- Expiry Date
- Oct 29, 2025
About this record
Access comprehensive regulatory information for “Geistlich” Fibro-Gide Collagen Matrix in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f0878a3c2e155e173b744817aff7ffb7 and manufactured by GEISTLICH PHARMA AG. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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