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“Arthesys” MAYA PTCA Catheter - Taiwan Registration 2adb5650abd4dde8101914a26549d370

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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2adb5650abd4dde8101914a26549d370
Registration Details
Taiwan FDA Registration: 2adb5650abd4dde8101914a26549d370
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Device Details

“Arthesys” MAYA PTCA Catheter
TW: “雅瑟斯”瑪亞冠狀動脈導管
Risk Class 3
MD

Registration Details

2adb5650abd4dde8101914a26549d370

Ministry of Health Medical Device Import No. 029423

DHA05602942302

Company Information

France

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E0005 Percutaneous puncture of the coronary ductus

Imported from abroad

Dates and Status

Mar 27, 2017

Mar 27, 2022