HUMIDAIR CLEANABLE - FDA Registration 18d3b54d0fca9d015e5db3794b29c67b
Access comprehensive regulatory information for HUMIDAIR CLEANABLE in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 18d3b54d0fca9d015e5db3794b29c67b and manufactured by ResMed Pty Ltd. The device was registered on February 18, 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
18d3b54d0fca9d015e5db3794b29c67b
HUMIDAIR CLEANABLE
FDA ID: 18d3b54d0fca9d015e5db3794b29c67b
Device Classification
Brand Name
ResMed
Registration Information
Analysis ID
18d3b54d0fca9d015e5db3794b29c67b
Registration Date
February 18, 2022
Manufacturer
Name
ResMed Pty LtdAuthorized Representative

