Philippines FDA registration CMDR-2025-04907A

LOGIQ P9 Ultrasound System

Philippines flagPhilippines·GE Ultrasound Korea, Ltd. - 9 Sunhwan-ro, 214beon-gil, Jungwon-gu, Seongnam-si, Gyeonggi-do, 13204 Republic of Korea·Korea·Issued June 26, 2025 – June 26, 2030
Device information
Product Name
LOGIQ P9 Ultrasound System
Registration Number
CMDR-2025-04907A
Manufacturer details
Country of Origin
Korea
Importer & distribution
Registration dates
Issuance Date
June 26, 2025
Expiry Date
June 26, 2030
About this record

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.

Free DatabasePowered by Pure Global AIFDA Official DataKorea