Cellpack DFL - FDA Registration e740583c1c2ac0752d87ae10a63a0296

Access comprehensive regulatory information for Cellpack DFL in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e740583c1c2ac0752d87ae10a63a0296 and manufactured by Sysmex Asia Pacific Pte Ltd.. The device was registered on May 02, 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.