ARCHITECT Rubella IgM Reagent Kit - FDA Registration b1fffbcfc5e0a069ad7b3d7e24cea9b0

Access comprehensive regulatory information for ARCHITECT Rubella IgM Reagent Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b1fffbcfc5e0a069ad7b3d7e24cea9b0 and manufactured by Abbott Ireland Diagnostics Division. The device was registered on February 05, 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.