Taiwan FDA registration e3de6bc2394e60c896c9ccb30ecf7181
“Hexacath” Premounted Coronary Stent HELIX
TW: “海斯凱”海力士冠狀動脈支架系統
Taiwan·Risk Class 3·MD·HEXACATH·Registered Jan 21, 2016 – Jan 21, 2021ExpiredRegistration details
- Analysis ID
- e3de6bc2394e60c896c9ccb30ecf7181
- License Form
- Ministry of Health Medical Device Import No. 028152
- Customs Code
- DHA05602815202
Company information
- Manufacturer
- HEXACATH
- Manufacturer Country
- France
- Authorized Representative
- WATTCAN INSTRUMENTS 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 21, 2016
- Expiry Date
- Jan 21, 2021
About this record
Access comprehensive regulatory information for “Hexacath” Premounted Coronary Stent HELIX in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e3de6bc2394e60c896c9ccb30ecf7181 and manufactured by HEXACATH. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
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