Diagnostic Ultrasound System - FDA Registration 7c0a38fb9470fbe585b5349e7e4c1c59
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 7c0a38fb9470fbe585b5349e7e4c1c59 and manufactured by Konica Minolta INC. The device was registered on September 09, 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
7c0a38fb9470fbe585b5349e7e4c1c59
Diagnostic Ultrasound System
FDA ID: 7c0a38fb9470fbe585b5349e7e4c1c59
Device Classification
Brand Name
Konica Minolta
Registration Information
Analysis ID
7c0a38fb9470fbe585b5349e7e4c1c59
Registration Date
September 09, 2022
Manufacturer
Authorized Representative

