Taiwan FDA registration 929debe66c126f63987b94cfa55934f1
"Baonan" Armstrong posterior spinal fixation system
TW: “寶楠”阿姆斯壯脊椎後路固定系統
Taiwan·Risk Class 2·PAONAN BIOTECH CO., LTD.·Registered Mar 29, 2013 – Mar 29, 2028ActiveRegistration details
- Analysis ID
- 929debe66c126f63987b94cfa55934f1
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 Orthopedics
- Product Type (Level 2)
- N.3070 椎弓螺釘系統
- Import Information
- Domestic
Dates and status
- Registration Date
- Mar 29, 2013
- Expiry Date
- Mar 29, 2028
About this record
Access comprehensive regulatory information for "Baonan" Armstrong posterior spinal fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 929debe66c126f63987b94cfa55934f1 and manufactured by PAONAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PAONAN BIOTECH CO., LTD..
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