Electrocardiograph - FDA Registration 56c0713a5a348f5e7848437c7371d501
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 56c0713a5a348f5e7848437c7371d501 and manufactured by Shenzhen Carewell Electronics Co., Ltd.. The device was registered on September 27, 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
56c0713a5a348f5e7848437c7371d501
Electrocardiograph
FDA ID: 56c0713a5a348f5e7848437c7371d501
Device Classification
Brand Name
Carewell
Registration Information
Analysis ID
56c0713a5a348f5e7848437c7371d501
Registration Date
September 27, 2022
Manufacturer
Authorized Representative

