Taiwan FDA registration 47ea8816405fb96f25f49d0c33a744aa
Linqi artificial replacement bone
TW: 琳悧人工替代骨
Taiwan·Risk Class 2·ZHENPENG BIOTECH CO., LTD.·Registered Feb 02, 2023 – Jun 22, 2029ActiveRegistration details
- Analysis ID
- 47ea8816405fb96f25f49d0c33a744aa
Company information
- Manufacturer
- ZHENPENG BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LINLI CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3045 Absorbable Calcium Salt Bone Cavity Filling Device
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Feb 02, 2023
- Expiry Date
- Jun 22, 2029
About this record
Access comprehensive regulatory information for Linqi artificial replacement bone in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 47ea8816405fb96f25f49d0c33a744aa and manufactured by ZHENPENG BIOTECH CO., LTD.. The authorized representative in Taiwan is LINLI CO., LTD..
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