SUPER TORQUE ® PLUS Diagnostic Catheter - FDA Registration MDR-01442

Access comprehensive regulatory information for SUPER TORQUE ® PLUS Diagnostic Catheter in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01442 and manufactured by Cordis US Corp.- 14201 North West 60th Avenue, Miami Lakes, Florida, 33014 USA mfd by: Cardinal Health Mexico 244 S.de R.L.de C.V- Santiago Troncoso 808 Parque Industrial Salvacar Ciudad Juarez Chihuahua CP 32574 Mexico in Mexico. The device was registered on March 10, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Getz Bros. Philippines, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.