ARCHITECT Rubella IgG Assay - FDA Registration d22953b981e2aa7c9c5c84beef1ef4c7

Access comprehensive regulatory information for ARCHITECT Rubella IgG Assay in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d22953b981e2aa7c9c5c84beef1ef4c7 and manufactured by Abbott Ireland Diagnostics Division. The device was registered on January 19, 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.