"Baxter" tissue repair coagulant spray tube - Taiwan Registration fa04901ca763acc0c9e8a697eabad256

Access comprehensive regulatory information for "Baxter" tissue repair coagulant spray tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fa04901ca763acc0c9e8a697eabad256 and manufactured by Made (部分製程) in POLAND;; Baxter Healthcare SA;; Baxter S.A.. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Clinico Medical Sp. z o.o.;; Baxter Healthcare SA, and 1 recent registrations in the same category. 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.