Philippines FDA registration CMDR-2024-03005A

LOGIQ E10 Ultrasound System

Philippines·GE Medical Systems Ultrasound and Primary Care Diagnostics, LLC 9900 Innovation Drive Wauwatosa, WI 53226 USA Mfd By: GE Ultrasound Korea, Ltd. - 9 Sunhwan-ro, 214beon-gil, Jungwon-gu, Seongnam-si, Gyeonggi-do, 13204 Republic of Korea·USA·Issued June 14, 2024 – June 14, 2029

Device information

Product Name: LOGIQ E10 Ultrasound System
Registration Number: CMDR-2024-03005A

Manufacturer details

Manufacturer: GE Medical Systems Ultrasound and Primary Care Diagnostics, LLC 9900 Innovation Drive Wauwatosa, WI 53226 USA Mfd By: GE Ultrasound Korea, Ltd. - 9 Sunhwan-ro, 214beon-gil, Jungwon-gu, Seongnam-si, Gyeonggi-do, 13204 Republic of Korea
Country of Origin: USA

Importer & distribution

Importer/Distributor: General Electric Philippines, Inc.

Registration dates

Issuance Date: June 14, 2024
Expiry Date: June 14, 2029

About this record

Access comprehensive regulatory information for LOGIQ E10 Ultrasound System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-03005A and manufactured by GE Medical Systems Ultrasound and Primary Care Diagnostics, LLC 9900 Innovation Drive Wauwatosa, WI 53226 USA Mfd By: GE Ultrasound Korea, Ltd. - 9 Sunhwan-ro, 214beon-gil, Jungwon-gu, Seongnam-si, Gyeonggi-do, 13204 Republic of Korea in USA. 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.