Taiwan FDA registration c4f0a33b47713328675da4e63ac1dd52
“Paonan” PK High Tibial Osteotomy Correction System
TW: “寶楠”盤古高位脛骨截骨矯正系統
Taiwan·Risk Class 2·MD·PAONAN BIOTECH CO., LTD.·Registered Sep 20, 2018 – Sep 20, 2028ActiveRegistration details
- Analysis ID
- c4f0a33b47713328675da4e63ac1dd52
- License Form
- Ministry of Health Medical Device Manufacturing No. 006181
Company information
- Manufacturer
- PAONAN BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PAONAN BIOTECH CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3030 Single or multi-metal bone fixation device and accessories
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 20, 2018
- Expiry Date
- Sep 20, 2028
About this record
Access comprehensive regulatory information for “Paonan” PK High Tibial Osteotomy Correction System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c4f0a33b47713328675da4e63ac1dd52 and manufactured by PAONAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PAONAN BIOTECH CO., LTD..
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