ISE Electrolyte Analyzer (Erba Lyte Plus) - FDA Registration af33a41f7d0d3455d1dddeefc80db023
Access comprehensive regulatory information for ISE Electrolyte Analyzer (Erba Lyte Plus) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID af33a41f7d0d3455d1dddeefc80db023 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
af33a41f7d0d3455d1dddeefc80db023
ISE Electrolyte Analyzer (Erba Lyte Plus)
FDA ID: af33a41f7d0d3455d1dddeefc80db023
Device Classification
Brand Name
Erba Brand
Registration Information
Analysis ID
af33a41f7d0d3455d1dddeefc80db023
Registration Date
October 05, 2022
Manufacturer
Authorized Representative
Name
AMTT CO., LTD
