Us2.v1 - AI software for echocardiography - FDA Registration CMDR-2025-04145

Access comprehensive regulatory information for Us2.v1 - AI software for echocardiography in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04145 and manufactured by EKO.AI Pte Ltd. 2 College Road, 02-00, 169 850 Singapore in Singapore. The device was registered on May 09, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Qualtech Manila Consulting Corporation), 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.