OZOTEX RF - FDA Registration 09e366e693d190e6d3209282d9dcc0cc
Access comprehensive regulatory information for OZOTEX RF in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 09e366e693d190e6d3209282d9dcc0cc and manufactured by Medsource Ozone Biomedicals Pvt. Ltd. The device was registered on October 15, 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
09e366e693d190e6d3209282d9dcc0cc
OZOTEX RF
FDA ID: 09e366e693d190e6d3209282d9dcc0cc
Device Classification
Brand Name
MEDSOURCE
Registration Information
Analysis ID
09e366e693d190e6d3209282d9dcc0cc
Registration Date
October 15, 2022
Manufacturer
Authorized Representative

