Response® 910 - FDA Registration 39d6a0d451612919d7bf370cf7a37260

Access comprehensive regulatory information for Response® 910 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 39d6a0d451612919d7bf370cf7a37260 and manufactured by DiaSys Diagnostic Systems GmbH. The device was registered on March 29, 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.