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Xpert HIV-1 Qual XC - FDA Registration 8ca4b5eb421b1ea4f1f1240aff005884

Access comprehensive regulatory information for Xpert HIV-1 Qual XC in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8ca4b5eb421b1ea4f1f1240aff005884 and manufactured by Cepheid AB. The device was registered on April 19, 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
8ca4b5eb421b1ea4f1f1240aff005884
Xpert HIV-1 Qual XC
FDA ID: 8ca4b5eb421b1ea4f1f1240aff005884
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Device Classification
Brand Name
Cepheid
Registration Information
Analysis ID
8ca4b5eb421b1ea4f1f1240aff005884
Registration Date
April 19, 2022
Manufacturer
Authorized Representative