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Reusable Resuscitator - FDA Registration 7be64d6ad5dcaa50f76d1ce42e596c79

Access comprehensive regulatory information for Reusable Resuscitator in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 7be64d6ad5dcaa50f76d1ce42e596c79 and manufactured by VADI Medical Technology Co.,Ltd. The device was registered on December 24, 2021.

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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7be64d6ad5dcaa50f76d1ce42e596c79
Reusable Resuscitator
FDA ID: 7be64d6ad5dcaa50f76d1ce42e596c79
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DJ Fang

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Device Classification
Brand Name
THE VALLEY
Registration Information
Analysis ID
7be64d6ad5dcaa50f76d1ce42e596c79
Registration Date
December 24, 2021
Authorized Representative