Taiwan FDA registration 2adb5650abd4dde8101914a26549d370
“Arthesys” MAYA PTCA Catheter
TW: “雅瑟斯”瑪亞冠狀動脈導管
Taiwan·Risk Class 3·MD·ARTHESYS·Registered Mar 27, 2017 – Mar 27, 2022ExpiredRegistration details
- Analysis ID
- 2adb5650abd4dde8101914a26549d370
- License Form
- Ministry of Health Medical Device Import No. 029423
- Customs Code
- DHA05602942302
Company information
- Manufacturer
- ARTHESYS
- Manufacturer Country
- France
- Authorized Representative
- HWA YI MEDICAL 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
- Mar 27, 2017
- Expiry Date
- Mar 27, 2022
About this record
Access comprehensive regulatory information for “Arthesys” MAYA PTCA Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2adb5650abd4dde8101914a26549d370 and manufactured by ARTHESYS. The authorized representative in Taiwan is HWA YI MEDICAL CO., LTD..
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