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AirSense10 - FDA Registration c175dfc0ecceaf13deb4abbe5cc90d14

Access comprehensive regulatory information for AirSense10 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c175dfc0ecceaf13deb4abbe5cc90d14 and manufactured by ResMed Pty Ltd. The device was registered on February 16, 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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c175dfc0ecceaf13deb4abbe5cc90d14
AirSense10
FDA ID: c175dfc0ecceaf13deb4abbe5cc90d14
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Device Classification
Brand Name
ResMed
Registration Information
Analysis ID
c175dfc0ecceaf13deb4abbe5cc90d14
Registration Date
February 16, 2022
Manufacturer
Authorized Representative