PULSE OXIMETER - FDA Registration eda96f025e3e59c3009db06bbf88474d
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 eda96f025e3e59c3009db06bbf88474d and manufactured by Edan Instruments, Inc.. The device was registered on March 30, 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
eda96f025e3e59c3009db06bbf88474d
PULSE OXIMETER
FDA ID: eda96f025e3e59c3009db06bbf88474d
Device Classification
Brand Name
Wacky
Registration Information
Analysis ID
eda96f025e3e59c3009db06bbf88474d
Registration Date
March 30, 2022
Manufacturer
Authorized Representative

