Taiwan FDA registration 5766d8e6b1b936ae25cb733491e21297
"Annica" multi-bone
TW: "憂尼卡"多扶骨
Taiwan·Risk Class 3·UNICARE BIOMEDICAL, INC.·Registered Nov 24, 2006 – Nov 24, 2026ActiveRegistration details
- Analysis ID
- 5766d8e6b1b936ae25cb733491e21297
- Customs Code
- DHA00601745108
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 Dentistry
- Product Type (Level 2)
- F.3930 Alveolar repair materials
- Import Information
- import
Dates and status
- Registration Date
- Nov 24, 2006
- Expiry Date
- Nov 24, 2026
About this record
Access comprehensive regulatory information for "Annica" multi-bone in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5766d8e6b1b936ae25cb733491e21297 and manufactured by UNICARE BIOMEDICAL, INC.. The authorized representative in Taiwan is HUNG KUO MEDICAL INSTRUMENT CO., LTD..
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