Taiwan FDA registration 13b91f0dc6384bd2c2c266c1eb0e9c17
"Atrien" Advanda V12 PTFE laminated bracket
TW: “亞翠恩”艾德凡達V12聚四氟乙烯 覆膜支架
Taiwan·Risk Class 3·Atrium Medical Corporation·Registered Jun 09, 2011 – Jun 09, 2026ExpiredRegistration details
- Analysis ID
- 13b91f0dc6384bd2c2c266c1eb0e9c17
- Customs Code
- DHA00602233704
Company information
- Manufacturer
- Atrium Medical Corporation
- Manufacturer Country
- United States
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Intended Use
- Details such as Chinese copy of the imitation order Efficiency change: Details such as the Chinese copy of the imitation of the approved version
- 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
- Jun 09, 2011
- Expiry Date
- Jun 09, 2026
About this record
Access comprehensive regulatory information for "Atrien" Advanda V12 PTFE laminated bracket in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 13b91f0dc6384bd2c2c266c1eb0e9c17 and manufactured by Atrium Medical Corporation. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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