Taiwan FDA registration 9ee05f6588d9b38bf6f6b96e840fcab0
"Baonan" non-polar interridge decompression system type I
TW: “寶楠”無極脊突間減壓系統I型
Taiwan·Risk Class 2·PAONAN BIOTECH CO., LTD.·Registered Mar 11, 2013 – Mar 11, 2028ActiveRegistration details
- Analysis ID
- 9ee05f6588d9b38bf6f6b96e840fcab0
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.3050 椎弓板間之脊椎矯正固定物
- Import Information
- Domestic
Dates and status
- Registration Date
- Mar 11, 2013
- Expiry Date
- Mar 11, 2028
About this record
Access comprehensive regulatory information for "Baonan" non-polar interridge decompression system type I in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ee05f6588d9b38bf6f6b96e840fcab0 and manufactured by PAONAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PAONAN BIOTECH CO., LTD..
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