Taiwan FDA registration bd1ea18fdd8c7aa353f92f696a015a81
“Paonan” Promise Lumbar Fusion System
TW: “寶楠”無極腰椎融合系統
Taiwan·Risk Class 2·MD·PAONAN BIOTECH CO., LTD.·Registered Oct 11, 2013 – Oct 11, 2028ActiveRegistration details
- Analysis ID
- bd1ea18fdd8c7aa353f92f696a015a81
- License Form
- Ministry of Health Medical Device Manufacturing No. 004229
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)
- N3050 Spine correction fixation between the peduncle plates
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 11, 2013
- Expiry Date
- Oct 11, 2028
About this record
Access comprehensive regulatory information for “Paonan” Promise Lumbar Fusion System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bd1ea18fdd8c7aa353f92f696a015a81 and manufactured by PAONAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PAONAN BIOTECH CO., LTD..
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