Pure Global AI
Myanmar FDA registration f017bfbc4cd10b763a1a9867db0b8dfe

ABX Pentra Precitest Solution

MyanmarHORIBAHORIBA ABX SASRegistered January 20, 2022
VerifiedFDA Myanmar · official registry
Device classification
Brand Name
HORIBA
Registration information
Analysis ID
f017bfbc4cd10b763a1a9867db0b8dfe
Registration Date
January 20, 2022
Manufacturer
Authorized Representative
About this record

Access comprehensive regulatory information for ABX Pentra Precitest Solution in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f017bfbc4cd10b763a1a9867db0b8dfe and manufactured by HORIBA ABX SAS. The device was registered on January 20, 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.