"Le Pulse" Putt aorta blocks the catheter - Taiwan Registration 81322e7316846942b9bc17d3338c110f
Access comprehensive regulatory information for "Le Pulse" Putt aorta blocks the catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 81322e7316846942b9bc17d3338c110f and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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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81322e7316846942b9bc17d3338c110f
Registration Details
Taiwan FDA Registration: 81322e7316846942b9bc17d3338c110f
Device Details
"Le Pulse" Putt aorta blocks the catheter
TW: โๆจ่โๆฎ็นไธปๅ่้ปๆทๅฐ็ฎก
Risk Class 2

