Taiwan FDA registration 5d15e5e36fac53eda366e76fdef11dd6
“Paonan” NEST-C Interbody System
TW: “寶楠”耐籠頸椎三維多孔鈦合金椎間融合器
Taiwan·Risk Class 2·MD·PAONAN BIOTECH CO., LTD.·Registered May 17, 2019 – May 17, 2024ExpiredRegistration details
- Analysis ID
- 5d15e5e36fac53eda366e76fdef11dd6
- License Form
- Ministry of Health Medical Device Manufacturing No. 006350
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 17, 2019
- Expiry Date
- May 17, 2024
About this record
Access comprehensive regulatory information for “Paonan” NEST-C 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 5d15e5e36fac53eda366e76fdef11dd6 and manufactured by PAONAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PAONAN BIOTECH CO., LTD..
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