AirStart 10 APAP - FDA Registration 4da6c122f232d421138f89ad3071cf76
Access comprehensive regulatory information for AirStart 10 APAP in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4da6c122f232d421138f89ad3071cf76 and manufactured by ResMed Pty Ltd. The device was registered on December 20, 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
4da6c122f232d421138f89ad3071cf76
AirStart 10 APAP
FDA ID: 4da6c122f232d421138f89ad3071cf76
Device Classification
Brand Name
ResMed
Registration Information
Analysis ID
4da6c122f232d421138f89ad3071cf76
Registration Date
December 20, 2022
Manufacturer
Name
ResMed Pty LtdAuthorized Representative

