Medonic M-series Diluent RFID - FDA Registration a485dbcd6a47271aeeef4eb199c83d60
Access comprehensive regulatory information for Medonic M-series Diluent RFID in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a485dbcd6a47271aeeef4eb199c83d60 and manufactured by Boule Medical AB. The device was registered on October 21, 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
a485dbcd6a47271aeeef4eb199c83d60
Medonic M-series Diluent RFID
FDA ID: a485dbcd6a47271aeeef4eb199c83d60
Device Classification
Brand Name
Medonic
Registration Information
Analysis ID
a485dbcd6a47271aeeef4eb199c83d60
Registration Date
October 21, 2022
Manufacturer
Name
Boule Medical ABAuthorized Representative

