Taiwan FDA registration 49d12f151d9b7529527a5277aa4dd557
“EucaTech” euca VI PTCA Balloon Catheter
TW: “優科德”優科第六代冠狀動脈氣球擴張導管
Taiwan·Risk Class 2·MD·eucatech AG·Registered Feb 05, 2018 – Feb 05, 2028ActiveRegistration details
- Analysis ID
- 49d12f151d9b7529527a5277aa4dd557
- License Form
- Ministry of Health Medical Device Import No. 030722
- Customs Code
- DHA05603072209
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)
- E0005 Percutaneous puncture of the coronary ductus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 05, 2018
- Expiry Date
- Feb 05, 2028
About this record
Access comprehensive regulatory information for “EucaTech” euca VI PTCA Balloon Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49d12f151d9b7529527a5277aa4dd557 and manufactured by eucatech AG. The authorized representative in Taiwan is SYNCESS CO., LTD..
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