"Termo" Akufoss coronary balloon dilation catheter - Taiwan Registration d1272115be69ccf87c007b752528fd1d
Access comprehensive regulatory information for "Termo" Akufoss coronary balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d1272115be69ccf87c007b752528fd1d and manufactured by TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN 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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d1272115be69ccf87c007b752528fd1d
Registration Details
Taiwan FDA Registration: d1272115be69ccf87c007b752528fd1d
Device Details
"Termo" Akufoss coronary balloon dilation catheter
TW: โๆณฐ็พ่โ้ฟ้
ทไฝๆฏๅ ็ๅ่ๆฑฝ็ๆดๅผตๅฐ็ฎก
Risk Class 3

