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Electrocardiovit - FDA Registration 9b22c1bbaa6be1dbed4a1713e71fa031

Access comprehensive regulatory information for Electrocardiovit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9b22c1bbaa6be1dbed4a1713e71fa031 and manufactured by Schiller AG. The device was registered on November 18, 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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9b22c1bbaa6be1dbed4a1713e71fa031
Electrocardiovit
FDA ID: 9b22c1bbaa6be1dbed4a1713e71fa031
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Device Classification
Brand Name
Schiller
Registration Information
Analysis ID
9b22c1bbaa6be1dbed4a1713e71fa031
Registration Date
November 18, 2022
Manufacturer
Authorized Representative