Cobas 4800 Cdiff Amplification/Detection Kit - FDA Registration 6cdb5033486c3584e6efc73c3f1526ec

Access comprehensive regulatory information for Cobas 4800 Cdiff Amplification/Detection Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6cdb5033486c3584e6efc73c3f1526ec and manufactured by Roche Molecular Systems, Inc.. The device was registered on November 18, 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.