Myanmar FDA registration ab11983dd09100cc7e99adb5f36090c4
LUMIS 150 VPAP ST ANZ TRI 4G
Myanmar·ResMed·ResMed Pty Ltd·Registered May 27, 2022Device classification
- Brand Name
- ResMed
Registration information
- Analysis ID
- ab11983dd09100cc7e99adb5f36090c4
- Registration Date
- May 27, 2022
Manufacturer
- Name
- ResMed Pty Ltd
Authorized Representative
About this record
Access comprehensive regulatory information for LUMIS 150 VPAP ST ANZ TRI 4G in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ab11983dd09100cc7e99adb5f36090c4 and manufactured by ResMed Pty Ltd. The device was registered on May 27, 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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