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Electrocardiograph - FDA Registration 63a1788329dc2afdebeb994329419e4e

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 63a1788329dc2afdebeb994329419e4e and manufactured by Schiller AG. The device was registered on February 01, 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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63a1788329dc2afdebeb994329419e4e
Electrocardiograph
FDA ID: 63a1788329dc2afdebeb994329419e4e
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Device Classification
Brand Name
Schiller
Registration Information
Analysis ID
63a1788329dc2afdebeb994329419e4e
Registration Date
February 01, 2022
Manufacturer
Authorized Representative