Auto Hematology Analyzer - FDA Registration f9f5aab9d0378b00c088053c7aebb483
Access comprehensive regulatory information for Auto Hematology Analyzer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f9f5aab9d0378b00c088053c7aebb483 and manufactured by B&E Bio-technology Co., Ltd. The device was registered on November 29, 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
f9f5aab9d0378b00c088053c7aebb483
Auto Hematology Analyzer
FDA ID: f9f5aab9d0378b00c088053c7aebb483
Device Classification
Brand Name
Hemax
Registration Information
Analysis ID
f9f5aab9d0378b00c088053c7aebb483
Registration Date
November 29, 2022
Manufacturer
Authorized Representative

