Taiwan FDA registration 7f18f847f3e6b728c87e7ea1546df3ee
“Clariance” Idys-LIF cages
TW: “克萊兒”艾迪斯腰椎融合器
Taiwan·Risk Class 2·MD·CLARIANCE·Registered Jun 26, 2018 – Jun 26, 2023ExpiredRegistration details
- Analysis ID
- 7f18f847f3e6b728c87e7ea1546df3ee
- License Form
- Ministry of Health Medical Device Import No. 031263
- Customs Code
- DHA05603126308
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)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 26, 2018
- Expiry Date
- Jun 26, 2023
About this record
Access comprehensive regulatory information for “Clariance” Idys-LIF cages in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f18f847f3e6b728c87e7ea1546df3ee and manufactured by CLARIANCE. The authorized representative in Taiwan is LI MIN BIOTECH CO., LTD..
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