ADVIA Centaur® System - FDA Registration 3c255cd49b842bda9e5a41d494aef3b3
Access comprehensive regulatory information for ADVIA Centaur® System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3c255cd49b842bda9e5a41d494aef3b3 and manufactured by Siemens Healthcare Diagnostics Inc. The device was registered on November 09, 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
3c255cd49b842bda9e5a41d494aef3b3
ADVIA Centaur® System
FDA ID: 3c255cd49b842bda9e5a41d494aef3b3
Device Classification
Brand Name
Siemens Brand
Registration Information
Analysis ID
3c255cd49b842bda9e5a41d494aef3b3
Registration Date
November 09, 2022
Manufacturer
Authorized Representative

