ADVIA Centaur® Acid/Base reagent for Centaur®/Centaur® XP - FDA Registration 10f80a5c91108d7bda122abb6e479091

Access comprehensive regulatory information for ADVIA Centaur® Acid/Base reagent for Centaur®/Centaur® XP in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 10f80a5c91108d7bda122abb6e479091 and manufactured by Siemens Healthcare Diagnostics Manufacturing Ltd.. 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.