Allia IGS 7 OR Interventional X-Ray System - FDA Registration CMDR-2025-04706B

Access comprehensive regulatory information for Allia IGS 7 OR Interventional X-Ray System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04706B and manufactured by GE Medical Systems SCS - 283 Rue De La Miniere 78530 Buc, France in France. The device was registered on June 17, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (General Electric 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.