ADVIA Centaur® System Reagents - FDA Registration be3b3efdb00f07ea3e28a3a8d0d3713b
Access comprehensive regulatory information for ADVIA Centaur® System Reagents in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID be3b3efdb00f07ea3e28a3a8d0d3713b and manufactured by Siemens Healthcare Diagnostics Inc. The device was registered on October 11, 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
be3b3efdb00f07ea3e28a3a8d0d3713b
ADVIA Centaur® System Reagents
FDA ID: be3b3efdb00f07ea3e28a3a8d0d3713b
Device Classification
Brand Name
Siemens Brand
Registration Information
Analysis ID
be3b3efdb00f07ea3e28a3a8d0d3713b
Registration Date
October 11, 2022
Manufacturer
Authorized Representative

