Handheld Pulse Oximeter - FDA Registration f5f55a0c1dd29b749e8dcf401035760d

Access comprehensive regulatory information for Handheld Pulse Oximeter in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f5f55a0c1dd29b749e8dcf401035760d and manufactured by Shenzhen Creative Industry Co., Ltd.. The device was registered on June 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.