Bioline HBsAg - FDA Registration 41434f1b437680ba716ca5184ee9f4b3
Access comprehensive regulatory information for Bioline HBsAg in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 41434f1b437680ba716ca5184ee9f4b3 and manufactured by Abbott Diagnostics Korea Inc.. The device was registered on October 28, 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.
Free Database
Powered by Pure Global AI
FDA Official Data
41434f1b437680ba716ca5184ee9f4b3
Bioline HBsAg
FDA ID: 41434f1b437680ba716ca5184ee9f4b3
Device Classification
Brand Name
Bioline
Registration Information
Analysis ID
41434f1b437680ba716ca5184ee9f4b3
Registration Date
October 28, 2022
Manufacturer
Authorized Representative

