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ELECTROCARDIOGRAPH - FDA Registration e185b7f6cb759cfe2fcaa62e1f7bad81

Access comprehensive regulatory information for ELECTROCARDIOGRAPH in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e185b7f6cb759cfe2fcaa62e1f7bad81 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
e185b7f6cb759cfe2fcaa62e1f7bad81
ELECTROCARDIOGRAPH
FDA ID: e185b7f6cb759cfe2fcaa62e1f7bad81
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Device Classification
Brand Name
Wacky
Registration Information
Analysis ID
e185b7f6cb759cfe2fcaa62e1f7bad81
Registration Date
March 30, 2022
Manufacturer
Authorized Representative