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REMstar Auto A-Flex, w/Humid System One 60 Series, INT - FDA Registration c9859160b817746c9dc99c6af145e17d

Access comprehensive regulatory information for REMstar Auto A-Flex, 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 c9859160b817746c9dc99c6af145e17d 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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c9859160b817746c9dc99c6af145e17d
REMstar Auto A-Flex, w/Humid System One 60 Series, INT
FDA ID: c9859160b817746c9dc99c6af145e17d
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Device Classification
Brand Name
PHILIPS RESPIRONICS
Registration Information
Analysis ID
c9859160b817746c9dc99c6af145e17d
Registration Date
April 26, 2022
Manufacturer
Authorized Representative