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BiPAP Auto BiFlex, w/Humid System One 60 Series, INT - FDA Registration b9644d9702c04075433a9e63354de1ef

Access comprehensive regulatory information for BiPAP Auto BiFlex, w/Humid System One 60 Series, INT in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b9644d9702c04075433a9e63354de1ef and manufactured by Respironics Inc.. The device was registered on April 26, 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
b9644d9702c04075433a9e63354de1ef
BiPAP Auto BiFlex, w/Humid System One 60 Series, INT
FDA ID: b9644d9702c04075433a9e63354de1ef
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DJ Fang

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Device Classification
Brand Name
PHILIPS RESPIRONICS
Registration Information
Analysis ID
b9644d9702c04075433a9e63354de1ef
Registration Date
April 26, 2022
Manufacturer
Authorized Representative