"Le Pulse" Neotel thrombus removal catheter - Taiwan Registration 1aeacaf94832fc061f8d3d8412d88d3c
Access comprehensive regulatory information for "Le Pulse" Neotel 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 1aeacaf94832fc061f8d3d8412d88d3c 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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1aeacaf94832fc061f8d3d8412d88d3c
Registration Details
Taiwan FDA Registration: 1aeacaf94832fc061f8d3d8412d88d3c
Device Details
"Le Pulse" Neotel thrombus removal catheter
TW: โๆจ่โๆฐ็น็พ่กๆ ๆธ
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Risk Class 2

