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Diagnostic Ultrasound System - FDA Registration b0f2a63e084fc49c664f93c21b1a3a90

Access comprehensive regulatory information for Diagnostic Ultrasound System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b0f2a63e084fc49c664f93c21b1a3a90 and manufactured by Shenzhen Mindray Bio-Medical Electronics Co.,Ltd.. The device was registered on November 16, 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
b0f2a63e084fc49c664f93c21b1a3a90
Diagnostic Ultrasound System
FDA ID: b0f2a63e084fc49c664f93c21b1a3a90
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Device Classification
Brand Name
Mindray
Registration Information
Analysis ID
b0f2a63e084fc49c664f93c21b1a3a90
Registration Date
November 16, 2022