Taiwan FDA registration bf5377ef9decbc6b07e983c8bb490295
“SHOFU” GLASIONOMER FX ULTRA
TW: “松風”奧創玻璃離子充填材
Taiwan·Risk Class 2·MD·SHOFU INC.·Registered May 26, 2017 – May 26, 2027ActiveRegistration details
- Analysis ID
- bf5377ef9decbc6b07e983c8bb490295
- License Form
- Ministry of Health Medical Device Import No. 029868
- Customs Code
- DHA05602986801
Company information
- Manufacturer
- SHOFU INC.
- Manufacturer Country
- Japan
- Authorized Representative
- SHOFU INC., TAIWAN BRANCH (JAPAN)
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
- May 26, 2017
- Expiry Date
- May 26, 2027
About this record
Access comprehensive regulatory information for “SHOFU” GLASIONOMER FX ULTRA in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf5377ef9decbc6b07e983c8bb490295 and manufactured by SHOFU INC.. The authorized representative in Taiwan is SHOFU INC., TAIWAN BRANCH (JAPAN).
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