"Le Pulse" Retis thrombus removal catheter - Taiwan Registration db842529e7939126a1d4957771dd1b23
Access comprehensive regulatory information for "Le Pulse" Retis 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 db842529e7939126a1d4957771dd1b23 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.
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db842529e7939126a1d4957771dd1b23
Registration Details
Taiwan FDA Registration: db842529e7939126a1d4957771dd1b23
Device Details
"Le Pulse" Retis thrombus removal catheter
TW: โๆจ่โ้ท็ทนๆฏ่กๆ ๆธ
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Risk Class 2

