APNEALINK AIR Complete set - FDA Registration 6d31aca0f4bc400a3389b18b798a5f62
Access comprehensive regulatory information for APNEALINK AIR Complete set in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6d31aca0f4bc400a3389b18b798a5f62 and manufactured by ResMed Pty Ltd. The device was registered on March 28, 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
6d31aca0f4bc400a3389b18b798a5f62
APNEALINK AIR Complete set
FDA ID: 6d31aca0f4bc400a3389b18b798a5f62
Device Classification
Brand Name
ResMed
Registration Information
Analysis ID
6d31aca0f4bc400a3389b18b798a5f62
Registration Date
March 28, 2022
Manufacturer
Name
ResMed Pty LtdAuthorized Representative

