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Dorma 500 Auto, INTL - FDA Registration a44e7a8ca15f3c76caf944059922c4a9

Access comprehensive regulatory information for Dorma 500 Auto, INTL in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a44e7a8ca15f3c76caf944059922c4a9 and manufactured by Respironics Inc.. The device was registered on March 23, 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
a44e7a8ca15f3c76caf944059922c4a9
Dorma 500 Auto, INTL
FDA ID: a44e7a8ca15f3c76caf944059922c4a9
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DJ Fang

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Device Classification
Brand Name
PHILIPS RESPIRONICS
Registration Information
Analysis ID
a44e7a8ca15f3c76caf944059922c4a9
Registration Date
March 23, 2022
Manufacturer
Authorized Representative