Xpert MTB/XDR - FDA Registration 7eee02dbc244bd99769f91e70b6a50e8
Access comprehensive regulatory information for Xpert MTB/XDR in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 7eee02dbc244bd99769f91e70b6a50e8 and manufactured by Cepheid. The device was registered on November 18, 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
7eee02dbc244bd99769f91e70b6a50e8
Xpert MTB/XDR
FDA ID: 7eee02dbc244bd99769f91e70b6a50e8
Device Classification
Brand Name
Cepheid
Registration Information
Analysis ID
7eee02dbc244bd99769f91e70b6a50e8
Registration Date
November 18, 2022
Manufacturer
Name
CepheidAuthorized Representative

