Patient Monitor - FDA Registration ea4ec06523c98c2b5fcea175a3c0bf1b

Access comprehensive regulatory information for Patient Monitor in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ea4ec06523c98c2b5fcea175a3c0bf1b and manufactured by Shenzhen Creative Industry Co., Ltd.. The device was registered on July 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.