Philippines FDA registration MDR-10652
PULMODYNE ACCUPAP POSITIVE AIRWAY PRESSURE THERAPY SYSTEM
Philippines·Pulmodyne, Inc. - Indiana, USA·USA·Issued December 28, 2020 – December 28, 2021Device information
- Product Name
- PULMODYNE ACCUPAP POSITIVE AIRWAY PRESSURE THERAPY SYSTEM
- Registration Number
- MDR-10652
Manufacturer details
- Manufacturer
- Pulmodyne, Inc. - Indiana, USA
- Country of Origin
- USA
Importer & distribution
- Importer/Distributor
- Panamed Philippines Inc.
Registration dates
- Issuance Date
- December 28, 2020
- Expiry Date
- December 28, 2021
About this record
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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