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OZOTEX RA - FDA Registration 892a3f98e4c91ce3a0c76b2a18109dca

Access comprehensive regulatory information for OZOTEX RA in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 892a3f98e4c91ce3a0c76b2a18109dca 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
892a3f98e4c91ce3a0c76b2a18109dca
OZOTEX RA
FDA ID: 892a3f98e4c91ce3a0c76b2a18109dca
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Device Classification
Brand Name
MEDSOURCE
Registration Information
Analysis ID
892a3f98e4c91ce3a0c76b2a18109dca
Registration Date
July 08, 2022