Taiwan FDA registration f8b4d11af4a8740fb9d4cc2a2e165ae1
“Eucatech” eucaLimus drug-eluting coronary stents
TW: “優科德”優科流明憘塗藥冠狀動脈血管支架
Taiwan·Risk Class 3·MD·eucatech AG·Registered Mar 08, 2019 – Mar 08, 2024ExpiredRegistration details
- Analysis ID
- f8b4d11af4a8740fb9d4cc2a2e165ae1
- License Form
- Ministry of Health Medical Device Import No. 032288
- Customs Code
- DHA05603228803
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
- Mar 08, 2019
- Expiry Date
- Mar 08, 2024
About this record
Access comprehensive regulatory information for “Eucatech” eucaLimus drug-eluting coronary stents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f8b4d11af4a8740fb9d4cc2a2e165ae1 and manufactured by eucatech AG. The authorized representative in Taiwan is SYNCESS CO., LTD..
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