Taiwan FDA registration 1f5d9b76e68009277e45f9661e96cf4f
“BioTai” Plus Intra-articular Injection
TW: “博爾泰”關節內注射劑
Taiwan·Risk Class 3·MD·MAXIGEN BIOTECH INC.·Registered Sep 14, 2017 – Aug 22, 2021CancelledRegistration details
- Analysis ID
- 1f5d9b76e68009277e45f9661e96cf4f
- License Form
- Ministry of Health Medical Device Manufacturing No. 005902
Company information
- Manufacturer
- MAXIGEN BIOTECH INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MAXIGEN BIOTECH INC.
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N0003 Hyaluronic acid implants for the joint cavity
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 14, 2017
- Expiry Date
- Aug 22, 2021
- Cancellation Date
- Aug 24, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “BioTai” Plus Intra-articular Injection in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1f5d9b76e68009277e45f9661e96cf4f and manufactured by MAXIGEN BIOTECH INC.. The authorized representative in Taiwan is MAXIGEN BIOTECH INC..
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