Philippines FDA registration CMDR-2025-05116

Vivid iq Ultrasound System

Name: Vivid iq Ultrasound System — Philippines FDA registration CMDR-2025-05116
Creator: GE Medical Systems (China) Co., Ltd. - No. 19, ChangJiang Road, Wuxi National Hi-Tech Dev. Zone 214028 Jiangsu, China
Keywords: Vivid iq Ultrasound System, CMDR-2025-05116, GE Medical Systems (China) Co., Ltd. - No. 19, ChangJiang Road, Wuxi National Hi-Tech Dev. Zone 214028 Jiangsu, China, General Electric Philippines, Inc., China, Philippines FDA registration

PhilippinesGE Medical Systems (China) Co., Ltd. - No. 19, ChangJiang Road, Wuxi National Hi-Tech Dev. Zone 214028 Jiangsu, ChinaChinaIssued July 17, 2025 – July 17, 2030

VerifiedFDA Philippines · official registry

Device information

Product Name: Vivid iq Ultrasound System
Registration Number: CMDR-2025-05116

Manufacturer details

Manufacturer: GE Medical Systems (China) Co., Ltd. - No. 19, ChangJiang Road, Wuxi National Hi-Tech Dev. Zone 214028 Jiangsu, China
Country of Origin: China

Importer & distribution

Importer/Distributor: General Electric Philippines, Inc.

Registration dates

Issuance Date: July 17, 2025
Expiry Date: July 17, 2030

About this record

Access comprehensive regulatory information for Vivid iq Ultrasound System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-05116 and manufactured by GE Medical Systems (China) Co., Ltd. - No. 19, ChangJiang Road, Wuxi National Hi-Tech Dev. Zone 214028 Jiangsu, China in China. The device was registered on July 17, 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.