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RESPICARE Nasal Oxygen Cannula - FDA Registration CMDR-2022-01149

Access comprehensive regulatory information for RESPICARE Nasal Oxygen Cannula in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2022-01149 and manufactured by SHENYANG RMS MEDICAL TECH CO., LTD. No. 21, Gaoke Road, Hunnan District Shenyang 110179 Liaoning, P.R. China in China. The device was registered on November 29, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (Iraseth Pharma, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.

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CMDR-2022-01149
RESPICARE Nasal Oxygen Cannula
Registered medical device in Philippines
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Device Information
Product Name
RESPICARE Nasal Oxygen Cannula
Registration Number
CMDR-2022-01149
Importer & Distribution
Importer/Distributor
Iraseth Pharma, Inc.
Registration Dates
Issuance Date
November 29, 2022
Expiry Date
November 29, 2027