AIRSENSE 10 AUTOSET - FDA Registration c3ec71d1f6770a54be8add004233c83a
Access comprehensive regulatory information for AIRSENSE 10 AUTOSET in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c3ec71d1f6770a54be8add004233c83a and manufactured by ResMed Pty Ltd. The device was registered on October 11, 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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FDA Official Data
c3ec71d1f6770a54be8add004233c83a
AIRSENSE 10 AUTOSET
FDA ID: c3ec71d1f6770a54be8add004233c83a
Device Classification
Brand Name
ResMed
Registration Information
Analysis ID
c3ec71d1f6770a54be8add004233c83a
Registration Date
October 11, 2022
Manufacturer
Name
ResMed Pty LtdAuthorized Representative

