"Carneca" percutaneous puncture of the coronary ductus - Taiwan Registration fb56eee5b427b1c81da55b9c161f2dbe

Access comprehensive regulatory information for "Carneca" percutaneous puncture of the coronary ductus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fb56eee5b427b1c81da55b9c161f2dbe and manufactured by KANEKA CORPORATION;; KANEKA CORPORATION OSAKA PLANT. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KANEKA MEDIX CORPORATION KANAGAWA PLANT, 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.