Taiwan FDA registration e7ef8646b23b73c86ad3ae89c9efdc6c

"Jiahong" Elico posterior spinal fixation system

TW: “佳鴻”伊莉克脊椎後路固定系統
Taiwan flagTaiwan·Risk Class 2·ALPHATEC SPINE INC.·Registered Oct 12, 2012 – Oct 12, 2022Cancelled
Registration details
Analysis ID
e7ef8646b23b73c86ad3ae89c9efdc6c
Customs Code
DHA00602405902
Company information
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.3070 椎弓螺釘系統
Import Information
import
Dates and status
Registration Date
Oct 12, 2012
Expiry Date
Oct 12, 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" Elico posterior spinal fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e7ef8646b23b73c86ad3ae89c9efdc6c and manufactured by ALPHATEC SPINE INC.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices