LDL-direct FL - FDA Registration 54876be2b598ff5e4959b0fb1552b75b
Access comprehensive regulatory information for LDL-direct FL in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 54876be2b598ff5e4959b0fb1552b75b and manufactured by Chema Diagnostica by Marco Fiore. The device was registered on November 30, 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
54876be2b598ff5e4959b0fb1552b75b
LDL-direct FL
FDA ID: 54876be2b598ff5e4959b0fb1552b75b
Device Classification
Brand Name
CHEMA DIAGNOSES
Registration Information
Analysis ID
54876be2b598ff5e4959b0fb1552b75b
Registration Date
November 30, 2022
Manufacturer
Authorized Representative

