ABX Lysebio - FDA Registration 159a1607d9fec2c03a6796ac999cd4c5
Access comprehensive regulatory information for ABX Lysebio in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 159a1607d9fec2c03a6796ac999cd4c5 and manufactured by HORIBA ABX SAS. The device was registered on April 05, 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
159a1607d9fec2c03a6796ac999cd4c5
ABX Lysebio
FDA ID: 159a1607d9fec2c03a6796ac999cd4c5
Device Classification
Brand Name
HORIBA
Registration Information
Analysis ID
159a1607d9fec2c03a6796ac999cd4c5
Registration Date
April 05, 2022
Manufacturer
Name
HORIBA ABX SASAuthorized Representative

