Autocal H - FDA Registration 640adc41d1c2703bebf63e30e3bae1a5
Access comprehensive regulatory information for Autocal H in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 640adc41d1c2703bebf63e30e3bae1a5 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
640adc41d1c2703bebf63e30e3bae1a5
Autocal H
FDA ID: 640adc41d1c2703bebf63e30e3bae1a5
Device Classification
Brand Name
Chema Diagnostica
Registration Information
Analysis ID
640adc41d1c2703bebf63e30e3bae1a5
Registration Date
November 30, 2022
Manufacturer
Authorized Representative

