Digital Ultrasonic Diagnostic Imaging System - FDA Registration e3095e61ab8468db7460359089a7f4a4
Access comprehensive regulatory information for Digital Ultrasonic Diagnostic Imaging System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e3095e61ab8468db7460359089a7f4a4 and manufactured by Shenzhen Mindray Bio Medical Electronics Co., Ltd. The device was registered on October 19, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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FDA Official Data
e3095e61ab8468db7460359089a7f4a4
Digital Ultrasonic Diagnostic Imaging System
FDA ID: e3095e61ab8468db7460359089a7f4a4
Device Classification
Brand Name
Mindray
Registration Information
Analysis ID
e3095e61ab8468db7460359089a7f4a4
Registration Date
October 19, 2022
Manufacturer
Authorized Representative

