Auto Haematology Analyzer - FDA Registration 79a255365542ab730eabe2b73275dba2
Access comprehensive regulatory information for Auto Haematology Analyzer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 79a255365542ab730eabe2b73275dba2 and manufactured by Shenzhen Dymind Biotechnology Co.,Ltd. The device was registered on March 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
79a255365542ab730eabe2b73275dba2
Auto Haematology Analyzer
FDA ID: 79a255365542ab730eabe2b73275dba2
Device Classification
Brand Name
DYMIND DH 36
Registration Information
Analysis ID
79a255365542ab730eabe2b73275dba2
Registration Date
March 14, 2022
Manufacturer
Authorized Representative

