careHPV® Test Kit - FDA Registration bf3d0034d0bf20d1a21d273c10c74fe6

Access comprehensive regulatory information for careHPV® Test Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID bf3d0034d0bf20d1a21d273c10c74fe6 and manufactured by QIAGEN (Shenzhen) Co. Ltd. The device was registered on November 25, 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.