Taiwan FDA registration 033db9bd3f457110508ded8567bf6416
“Unicare” CYTOFLEX Resorb
TW: “憂尼卡”麗收骨可吸收式再生薄膜
Taiwan·Risk Class 2·MD·UNICARE BIOMEDICAL, INC.·Registered Apr 24, 2018 – Apr 24, 2028ActiveRegistration details
- Analysis ID
- 033db9bd3f457110508ded8567bf6416
- License Form
- Ministry of Health Medical Device Import No. 031053
- Customs Code
- DHA05603105300
Company information
- Manufacturer
- UNICARE BIOMEDICAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- HUNG KUO MEDICAL INSTRUMENT CO., LTD.
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
- Apr 24, 2018
- Expiry Date
- Apr 24, 2028
About this record
Access comprehensive regulatory information for “Unicare” CYTOFLEX Resorb in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 033db9bd3f457110508ded8567bf6416 and manufactured by UNICARE BIOMEDICAL, INC.. The authorized representative in Taiwan is HUNG KUO MEDICAL INSTRUMENT CO., LTD..
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