Taiwan FDA registration b81c0de2157a5a6f53588bb1e04604fa
“Paonan” NEST Interbody System
TW: “寶楠”耐籠三維多孔鈦合金椎間融合器
Taiwan·Risk Class 2·MD·PAONAN BIOTECH CO., LTD.·Registered May 11, 2018 – May 11, 2028ActiveRegistration details
- Analysis ID
- b81c0de2157a5a6f53588bb1e04604fa
- License Form
- Ministry of Health Medical Device Manufacturing No. 006047
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)
- N3080 Interbody fusion device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 11, 2018
- Expiry Date
- May 11, 2028
About this record
Access comprehensive regulatory information for “Paonan” NEST Interbody System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b81c0de2157a5a6f53588bb1e04604fa and manufactured by PAONAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PAONAN BIOTECH CO., LTD..
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