Taiwan FDA registration 705857b95b7ac2ffbae031bd4d2500b3
“Hexacath” Premounted Coronary Stent TITAN OPTIMAX
TW: “海斯凱”泰坦歐德邁冠狀動脈支架系統
Taiwan·Risk Class 3·MD·HEXACATH·Registered Jan 18, 2016 – Jan 18, 2026ExpiredRegistration details
- Analysis ID
- 705857b95b7ac2ffbae031bd4d2500b3
- License Form
- Ministry of Health Medical Device Import No. 028148
- Customs Code
- DHA05602814801
Company information
- Manufacturer
- HEXACATH
- Manufacturer Country
- France
- Authorized Representative
- CATHERINE CONSULTANTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E0001 Cardiovascular stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 18, 2016
- Expiry Date
- Jan 18, 2026
About this record
Access comprehensive regulatory information for “Hexacath” Premounted Coronary Stent TITAN OPTIMAX in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 705857b95b7ac2ffbae031bd4d2500b3 and manufactured by HEXACATH. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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