Hematology Analyzer (ELite 580) - FDA Registration 9ab2ef16400abfe703f6f8cd0ad5b331
Access comprehensive regulatory information for Hematology Analyzer (ELite 580) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9ab2ef16400abfe703f6f8cd0ad5b331 and manufactured by Erba Lachema s.r.o.. The device was registered on October 05, 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
9ab2ef16400abfe703f6f8cd0ad5b331
Hematology Analyzer (ELite 580)
FDA ID: 9ab2ef16400abfe703f6f8cd0ad5b331
Device Classification
Brand Name
Erba Brand
Registration Information
Analysis ID
9ab2ef16400abfe703f6f8cd0ad5b331
Registration Date
October 05, 2022
Manufacturer
Authorized Representative
Name
AMTT CO., LTD
