"Ginos" percutaneous puncture angioplasty balloon dilation catheter - Taiwan Registration b6c6b02fbf59a19ae7bc4f277e7107d5
Access comprehensive regulatory information for "Ginos" percutaneous puncture angioplasty balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b6c6b02fbf59a19ae7bc4f277e7107d5 and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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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b6c6b02fbf59a19ae7bc4f277e7107d5
Registration Details
Taiwan FDA Registration: b6c6b02fbf59a19ae7bc4f277e7107d5
Device Details
"Ginos" percutaneous puncture angioplasty balloon dilation catheter
TW: โๅ่ซพๅธโ็ถ็ฎ็ฉฟๅบ่ก็ฎกๆๅฝข่ก็ๅๆดๅผตๅฐ็ฎก
Risk Class 2

