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Cardiopulmonary Resuscitation Device - FDA Registration 164b3b6f9545c8235205f65127b97670

Access comprehensive regulatory information for Cardiopulmonary Resuscitation Device in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 164b3b6f9545c8235205f65127b97670 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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164b3b6f9545c8235205f65127b97670
Cardiopulmonary Resuscitation Device
FDA ID: 164b3b6f9545c8235205f65127b97670
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Device Classification
Brand Name
Schiller
Registration Information
Analysis ID
164b3b6f9545c8235205f65127b97670
Registration Date
February 01, 2022
Manufacturer
Authorized Representative