Coagulation Factor XII Deficient Plasma - FDA Registration 5341ccbff3e48c10f442b972bf760a8f

Access comprehensive regulatory information for Coagulation Factor XII Deficient Plasma in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5341ccbff3e48c10f442b972bf760a8f and manufactured by Siemens Healthcare Diagnostics Products GmbH. The device was registered on December 14, 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.