H560 Hematology Analyser - FDA Registration 75a52c69cf996e7383796101e34d226c
Access comprehensive regulatory information for H560 Hematology Analyser in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 75a52c69cf996e7383796101e34d226c and manufactured by Erba Lachema s.r.o. The device was registered on May 18, 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
75a52c69cf996e7383796101e34d226c
H560 Hematology Analyser
FDA ID: 75a52c69cf996e7383796101e34d226c
Device Classification
Brand Name
Grass Mannheim
Registration Information
Analysis ID
75a52c69cf996e7383796101e34d226c
Registration Date
May 18, 2022
Manufacturer
Authorized Representative

