Xpert HPV - FDA Registration 2cef155ee170c772d714242f8d213d0a
Access comprehensive regulatory information for Xpert HPV in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2cef155ee170c772d714242f8d213d0a and manufactured by Cepheid AB. The device was registered on April 05, 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
2cef155ee170c772d714242f8d213d0a
Xpert HPV
FDA ID: 2cef155ee170c772d714242f8d213d0a
Device Classification
Brand Name
GeneXpert
Registration Information
Analysis ID
2cef155ee170c772d714242f8d213d0a
Registration Date
April 05, 2022
Manufacturer
Name
Cepheid ABAuthorized Representative

