Taiwan FDA registration fde36dbf618de48dd5f6c2ce84ce9576
"Jiahong" Noo intervertebral fusion device
TW: “佳鴻”諾歐椎間融合器
Taiwan·Risk Class 2·ALPHATEC SPINE INC.·Registered Sep 25, 2012 – Sep 25, 2022CancelledRegistration details
- Analysis ID
- fde36dbf618de48dd5f6c2ce84ce9576
- Customs Code
- DHA00602404402
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
- Sep 25, 2012
- Expiry Date
- Sep 25, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Jiahong" Noo 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 fde36dbf618de48dd5f6c2ce84ce9576 and manufactured by ALPHATEC SPINE INC.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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