Quintus™ 5-Part Diluent - FDA Registration 8f6aa3b088ef9399854a872fe8150629

Access comprehensive regulatory information for Quintus™ 5-Part Diluent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8f6aa3b088ef9399854a872fe8150629 and manufactured by Clinical Diagnostic Solutions, Inc.. The device was registered on November 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.