Philippines FDA registration CMDR-2024-03004

LOGIQ P8 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 14, 2024 – June 14, 2029
Device information
Product Name
LOGIQ P8 Ultrasound System
Registration Number
CMDR-2024-03004
Manufacturer details
Country of Origin
Korea
Importer & distribution
Registration dates
Issuance Date
June 14, 2024
Expiry Date
June 14, 2029
About this record

Access comprehensive regulatory information for LOGIQ P8 Ultrasound System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-03004 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 14, 2024.

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.

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