LOGIQ P9 Ultrasound System - FDA Registration CMDR-2025-04907A

Access comprehensive regulatory information for LOGIQ P9 Ultrasound System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04907A and manufactured by GE Ultrasound Korea, Ltd. - 9 Sunhwan-ro, 214beon-gil, Jungwon-gu, Seongnam-si, Gyeonggi-do, 13204 Republic of Korea in Korea. The device was registered on June 26, 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.