Ultra HDL (ARCHITECT) - FDA Registration c229470f61a7114603c6171a0fc60023

Access comprehensive regulatory information for Ultra HDL (ARCHITECT) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c229470f61a7114603c6171a0fc60023 and manufactured by Sekisui Diagnostics P.E.I. Inc.. The device was registered on October 06, 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.