Taiwan FDA registration 17e507a091752e4c2b6103be799630ac
“EucaTech” euca AC Aspiration Catheter
TW: “優科德”優科愛喜吸除導管
Taiwan·Risk Class 2·MD·eucatech AG·Registered Dec 19, 2017 – Dec 19, 2027ActiveRegistration details
- Analysis ID
- 17e507a091752e4c2b6103be799630ac
- License Form
- Ministry of Health Medical Device Import No. 030621
- Customs Code
- DHA05603062103
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)
- E5150 Thrombectomy catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 19, 2017
- Expiry Date
- Dec 19, 2027
About this record
Access comprehensive regulatory information for “EucaTech” euca AC Aspiration Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17e507a091752e4c2b6103be799630ac and manufactured by eucatech AG. The authorized representative in Taiwan is SYNCESS CO., LTD..
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