PULMODYNE ACCUPAP POSITIVE AIRWAY PRESSURE THERAPY SYSTEM - FDA Registration MDR-10652
Access comprehensive regulatory information for PULMODYNE ACCUPAP POSITIVE AIRWAY PRESSURE THERAPY SYSTEM in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10652 and manufactured by Pulmodyne, Inc. - Indiana, USA in USA. The device was registered on December 28, 2020.
This page provides complete registration details including manufacturer information, importer/distributor details (Panamed Philippines 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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MDR-10652
PULMODYNE ACCUPAP POSITIVE AIRWAY PRESSURE THERAPY SYSTEM
Registered medical device in Philippines
Device Information
Product Name
PULMODYNE ACCUPAP POSITIVE AIRWAY PRESSURE THERAPY SYSTEM
Registration Number
MDR-10652
Manufacturer Details
Manufacturer
Pulmodyne, Inc. - Indiana, USACountry of Origin
USA
Importer & Distribution
Importer/Distributor
Panamed Philippines Inc.Registration Dates
Issuance Date
December 28, 2020
Expiry Date
December 28, 2021

