Kii® Balloon Blunt Tip System - FDA Registration CMDR-2025-04480

Access comprehensive regulatory information for Kii® Balloon Blunt Tip System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04480 and manufactured by Applied Medical Resources Corporation 22872 Avenida Empresa, Rancho Santa Margarita CA 92688, USA in USA. The device was registered on May 06, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (RBGM Medical Express Sales, 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.