3 Channel ECG Machine - FDA Registration dd3545d6503084edcaf2ad76bf5ee87b
Access comprehensive regulatory information for 3 Channel ECG Machine in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID dd3545d6503084edcaf2ad76bf5ee87b and manufactured by Guangdong Biolight Meditech Co.,Ltd.. The device was registered on January 28, 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
dd3545d6503084edcaf2ad76bf5ee87b
3 Channel ECG Machine
FDA ID: dd3545d6503084edcaf2ad76bf5ee87b
Device Classification
Brand Name
Biolight
Registration Information
Analysis ID
dd3545d6503084edcaf2ad76bf5ee87b
Registration Date
January 28, 2022
Manufacturer
Authorized Representative

