ABX Pentra MultiControl - FDA Registration 66876739f8bb8dd8e847a818e68e35b1
Access comprehensive regulatory information for ABX Pentra MultiControl in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 66876739f8bb8dd8e847a818e68e35b1 and manufactured by Roche Diagnostics GmbH Roche Life Science. The device was registered on December 14, 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
66876739f8bb8dd8e847a818e68e35b1
ABX Pentra MultiControl
FDA ID: 66876739f8bb8dd8e847a818e68e35b1
Device Classification
Brand Name
HORIBA
Registration Information
Analysis ID
66876739f8bb8dd8e847a818e68e35b1
Registration Date
December 14, 2022
Manufacturer
Authorized Representative

