"Le Pulse" Retius coaxial lead thrombus removal catheter - Taiwan Registration e6dffd1c37854fbfddba7bcf62b836f5
Access comprehensive regulatory information for "Le Pulse" Retius coaxial lead thrombus removal catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e6dffd1c37854fbfddba7bcf62b836f5 and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is HSIN TUNG 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.
Free Database
Powered by Pure Global AI
89,000+ Devices
e6dffd1c37854fbfddba7bcf62b836f5
Registration Details
Taiwan FDA Registration: e6dffd1c37854fbfddba7bcf62b836f5
Device Details
"Le Pulse" Retius coaxial lead thrombus removal catheter
TW: โๆจ่โ้ท็ทนๆฏๅ่ปธๅฐ็ท่กๆ ๆธ
้คๅฐ็ฎก
Risk Class 2

