Taiwan FDA registration 50dc5a8154b8366bbfa7af5a89502ad2
"Avatek" No-O Intervertebral Fusion Device
TW: "阿伐泰克" 諾歐椎間融合器
Taiwan·Risk Class 2·ALPHATEC SPINE INC.·Registered Jan 25, 2013 – Jan 25, 2023ExpiredRegistration details
- Analysis ID
- 50dc5a8154b8366bbfa7af5a89502ad2
- Customs Code
- DHA00602462302
Company information
- Manufacturer
- ALPHATEC SPINE INC.
- Manufacturer Country
- United States
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3060 椎體間之脊椎矯正固定物
- Import Information
- import
Dates and status
- Registration Date
- Jan 25, 2013
- Expiry Date
- Jan 25, 2023
About this record
Access comprehensive regulatory information for "Avatek" No-O Intervertebral Fusion Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50dc5a8154b8366bbfa7af5a89502ad2 and manufactured by ALPHATEC SPINE INC.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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