Taiwan FDA registration 2e160279058d6591d6926313539ee49a
"Eliser" Diser second generation coronary artery coating stent system
TW: “依莉瑟”迪瑟第二代冠狀動脈塗藥支架系統
Taiwan·Risk Class 3·Acon Regulatory Consultancy Services Ltd;; Elixir Medical Corporation·Registered Oct 10, 2018 – Oct 10, 2028ActiveRegistration details
- Analysis ID
- 2e160279058d6591d6926313539ee49a
- Customs Code
- DHA05603183300
Company information
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- WONDERVILLE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0001 Cardiovascular stents
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Oct 10, 2018
- Expiry Date
- Oct 10, 2028
About this record
Access comprehensive regulatory information for "Eliser" Diser second generation coronary artery coating stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2e160279058d6591d6926313539ee49a and manufactured by Acon Regulatory Consultancy Services Ltd;; Elixir Medical Corporation. The authorized representative in Taiwan is WONDERVILLE CO., LTD..
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