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Vivid iq Ultrasound System - FDA Registration CMDR-2025-05116

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.

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CMDR-2025-05116
Vivid iq Ultrasound System
Registered medical device in Philippines
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Device Information
Product Name
Vivid iq Ultrasound System
Registration Number
CMDR-2025-05116
Importer & Distribution
Registration Dates
Issuance Date
July 17, 2025
Expiry Date
July 17, 2030