OZOTEX RPR - FDA Registration d1627c705074cd0abaa0d7c26e862916
Access comprehensive regulatory information for OZOTEX RPR in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d1627c705074cd0abaa0d7c26e862916 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
d1627c705074cd0abaa0d7c26e862916
OZOTEX RPR
FDA ID: d1627c705074cd0abaa0d7c26e862916
Device Classification
Brand Name
MEDSOURCE
Registration Information
Analysis ID
d1627c705074cd0abaa0d7c26e862916
Registration Date
July 08, 2022
Manufacturer
Authorized Representative

