Taiwan FDA registration 1390e3cb4acd67d579af82160213911e
“EucaTech” euca CCFlex Coronary Stent System
TW: “優科德”優科喜福來冠狀動脈支架系統
Taiwan·Risk Class 3·MD·eucatech AG·Registered Sep 10, 2018 – Sep 10, 2028ActiveRegistration details
- Analysis ID
- 1390e3cb4acd67d579af82160213911e
- License Form
- Ministry of Health Medical Device Import No. 031520
- Customs Code
- DHA05603152002
Company information
- Manufacturer
- eucatech AG
- Manufacturer Country
- Germany
- Authorized Representative
- SYNCESS 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
- Sep 10, 2018
- Expiry Date
- Sep 10, 2028
About this record
Access comprehensive regulatory information for “EucaTech” euca CCFlex Coronary 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 1390e3cb4acd67d579af82160213911e and manufactured by eucatech AG. The authorized representative in Taiwan is SYNCESS CO., LTD..
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