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OZOTEX ASO - FDA Registration c6be69203e2962231422410a6d9faf41

Access comprehensive regulatory information for OZOTEX ASO in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c6be69203e2962231422410a6d9faf41 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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c6be69203e2962231422410a6d9faf41
OZOTEX ASO
FDA ID: c6be69203e2962231422410a6d9faf41
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Device Classification
Brand Name
MEDSOURCE
Registration Information
Analysis ID
c6be69203e2962231422410a6d9faf41
Registration Date
July 08, 2022