KAGE PEEK Interbody Cage - Taiwan Registration 817597348f422222e2abd508afbefc30
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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Device Details
Registration Details
817597348f422222e2abd508afbefc30
Ministry of Health Medical Device Manufacturing No. 006911
Product Details
For details, it is Chinese approved copy of the imitation order
N Orthopedic devices
N3080 Interbody fusion device
Produced in Taiwan, China
Dates and Status
Jul 16, 2020
Jul 16, 2025