Mobile C-arm X-Ray System - FDA Registration d2c567d1ef7c756dd1ece9a15d1a6056
Access comprehensive regulatory information for Mobile C-arm X-Ray System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d2c567d1ef7c756dd1ece9a15d1a6056 and manufactured by Siemens Healthcare GmbH. The device was registered on December 29, 2021.
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
d2c567d1ef7c756dd1ece9a15d1a6056
Mobile C-arm X-Ray System
FDA ID: d2c567d1ef7c756dd1ece9a15d1a6056
Device Classification
Brand Name
Siemens
Registration Information
Analysis ID
d2c567d1ef7c756dd1ece9a15d1a6056
Registration Date
December 29, 2021
Manufacturer
Authorized Representative

