Taiwan FDA registration 4f1c1f5cef8a8b7d6d81c113dc4cbad1
“Paonan” Rocket Interspinous Process System
TW: “寶楠”洛克脊突間減壓系統
Taiwan·Risk Class 2·MD·PAONAN BIOTECH CO., LTD.·Registered Apr 20, 2023 – Apr 20, 2028ActiveRegistration details
- Analysis ID
- 4f1c1f5cef8a8b7d6d81c113dc4cbad1
- License Form
- Ministry of Health Medical Device Manufacturing No. 007856
Company information
- Manufacturer
- PAONAN BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PAONAN BIOTECH CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N3050 Spine correction fixation between the peduncle plates
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Apr 20, 2023
- Expiry Date
- Apr 20, 2028
About this record
Access comprehensive regulatory information for “Paonan” Rocket Interspinous Process System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4f1c1f5cef8a8b7d6d81c113dc4cbad1 and manufactured by PAONAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PAONAN BIOTECH CO., LTD..
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