Taiwan FDA registration 817597348f422222e2abd508afbefc30
KAGE PEEK Interbody Cage
TW: 鎧基高分子椎間融合器
Taiwan·Risk Class 2·MD·CHANPIN MEDTAK CO., LTD.·Registered Jul 16, 2020 – Jul 16, 2025ExpiredRegistration details
- Analysis ID
- 817597348f422222e2abd508afbefc30
- License Form
- Ministry of Health Medical Device Manufacturing No. 006911
Company information
- Manufacturer
- CHANPIN MEDTAK CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- CHANPIN MEDTAK 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
- Jul 16, 2020
- Expiry Date
- Jul 16, 2025
About this record
Access comprehensive regulatory information for KAGE PEEK Interbody Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 817597348f422222e2abd508afbefc30 and manufactured by CHANPIN MEDTAK CO., LTD.. The authorized representative in Taiwan is CHANPIN MEDTAK CO., LTD..
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