Pulse Oximeter - FDA Registration 22e27ca3761fed43044369362674d0a0
Access comprehensive regulatory information for Pulse Oximeter in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 22e27ca3761fed43044369362674d0a0 and manufactured by Beijing Choice Electronic Technology Co., Ltd, People's Republic of China. The device was registered on October 20, 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.
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FDA Official Data
22e27ca3761fed43044369362674d0a0
Pulse Oximeter
FDA ID: 22e27ca3761fed43044369362674d0a0
Device Classification
Brand Name
ChoiceMMed
Registration Information
Analysis ID
22e27ca3761fed43044369362674d0a0
Registration Date
October 20, 2022
Authorized Representative

