"Kubota" Blood Bank Centrifuge for In Vitro Diagnostic Use (Non-Sterile) - Taiwan Registration 09db44d97831e92a856733fc2a174448

Access comprehensive regulatory information for "Kubota" Blood Bank Centrifuge for In Vitro Diagnostic Use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 09db44d97831e92a856733fc2a174448 and manufactured by KUBOTA MFG. CORP. FUJIOKA PLANT. The authorized representative in Taiwan is DOUBLE EAGLE ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KUBOTA MFG. CORP. FUJIOKA 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.