Xpert Vaginal/Endocervical Specimen Collection Kit - FDA Registration 1f3d39c8561f1ab06113593f470b5187

Access comprehensive regulatory information for Xpert Vaginal/Endocervical Specimen Collection Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1f3d39c8561f1ab06113593f470b5187 and manufactured by Cepheid. The device was registered on April 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.