"Gore" sealing valve Frix guide sheath - Taiwan Registration d137054eaacfa99f9c14b0aebf238572
Access comprehensive regulatory information for "Gore" sealing valve Frix guide sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d137054eaacfa99f9c14b0aebf238572 and manufactured by Creganna Medical;; W.L. Gore & Associates, Inc.. The authorized representative in Taiwan is W.L. GORE & ASSOCIATES (HONG KONG) LTD. TAIWAN BRANCH (H.K.).
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.
Device Details
Registration Details
d137054eaacfa99f9c14b0aebf238572
DHA05603261202
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular Medicine Science
E.1340 Catheter Introducers
Input;; Contract manufacturing
Dates and Status
May 24, 2019
May 24, 2029

