Pulse Oximeter (Hand Held Type) - FDA Registration 0b7b81aab3c5dd7c5583ccb496147926
Access comprehensive regulatory information for Pulse Oximeter (Hand Held Type) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0b7b81aab3c5dd7c5583ccb496147926 and manufactured by Bistos Co.,Ltd.. The device was registered on May 11, 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.
Free Database
Powered by Pure Global AI
FDA Official Data
0b7b81aab3c5dd7c5583ccb496147926
Pulse Oximeter (Hand Held Type)
FDA ID: 0b7b81aab3c5dd7c5583ccb496147926
Device Classification
Brand Name
bistos
Registration Information
Analysis ID
0b7b81aab3c5dd7c5583ccb496147926
Registration Date
May 11, 2022
Manufacturer
Name
Bistos Co.,Ltd.Authorized Representative

