NeuMoDx™ HIV-1 - FDA Registration 33011dc4dd5284d075ae0302495fc270

Access comprehensive regulatory information for NeuMoDx™ HIV-1 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 33011dc4dd5284d075ae0302495fc270 and manufactured by NeuMoDx Molecular, Inc.. The device was registered on June 08, 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.