OZOTEX WIDAL - FDA Registration 5001e1aee39c9819f63f7775d567d053
Access comprehensive regulatory information for OZOTEX WIDAL in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5001e1aee39c9819f63f7775d567d053 and manufactured by Medsource Ozone Biomedicals Pvt. Ltd.. The device was registered on July 08, 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
5001e1aee39c9819f63f7775d567d053
OZOTEX WIDAL
FDA ID: 5001e1aee39c9819f63f7775d567d053
Device Classification
Brand Name
MEDSOURCE
Registration Information
Analysis ID
5001e1aee39c9819f63f7775d567d053
Registration Date
July 08, 2022
Manufacturer
Authorized Representative

