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AIRFIT P10 MASK SYSTEM- APAC - FDA Registration 97dfca0eb7e32f754ff51557b8e90b3e

Access comprehensive regulatory information for AIRFIT P10 MASK SYSTEM- APAC in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 97dfca0eb7e32f754ff51557b8e90b3e and manufactured by ResMed Pty Ltd. The device was registered on January 24, 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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97dfca0eb7e32f754ff51557b8e90b3e
AIRFIT P10 MASK SYSTEM- APAC
FDA ID: 97dfca0eb7e32f754ff51557b8e90b3e
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Device Classification
Brand Name
ResMed
Registration Information
Analysis ID
97dfca0eb7e32f754ff51557b8e90b3e
Registration Date
January 24, 2022
Manufacturer
Authorized Representative