Taiwan FDA registration 3a0e4fdd9017fb507e425266f99a9e37

“Clariance” Idys-C cage cervical

TW: “克萊兒”艾迪斯頸椎融合器
Taiwan flagTaiwan·Risk Class 2·MD·CLARIANCE·Registered Nov 30, 2017 – Nov 30, 2022Expired
Registration details
Analysis ID
3a0e4fdd9017fb507e425266f99a9e37
License Form
Ministry of Health Medical Device Import No. 030573
Customs Code
DHA05603057305
Company information
Manufacturer
CLARIANCE
Manufacturer Country
France
Authorized Representative
LI MIN BIOTECH 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)
N3060 Spine correction fixation between vertebral bodies
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 30, 2017
Expiry Date
Nov 30, 2022
About this record

Access comprehensive regulatory information for “Clariance” Idys-C cage cervical in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3a0e4fdd9017fb507e425266f99a9e37 and manufactured by CLARIANCE. The authorized representative in Taiwan is LI MIN BIOTECH 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