HUDSON RCI® AQUAPAK® STERILE WATER AND NEBULIZER ADAPTOR - FDA Registration MDR-09669
Access comprehensive regulatory information for HUDSON RCI® AQUAPAK® STERILE WATER AND NEBULIZER ADAPTOR in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09669 and manufactured by Teleflex Medical in USA. The device was registered on May 13, 2020.
This page provides complete registration details including manufacturer information, importer/distributor details (IDS Medical Systems 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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USA
MDR-09669
HUDSON RCI® AQUAPAK® STERILE WATER AND NEBULIZER ADAPTOR
Registered medical device in Philippines
Device Information
Product Name
HUDSON RCI® AQUAPAK® STERILE WATER AND NEBULIZER ADAPTOR
Registration Number
MDR-09669
Manufacturer Details
Manufacturer
Teleflex MedicalCountry of Origin
USA
Importer & Distribution
Importer/Distributor
IDS Medical Systems Philippines, Inc.Registration Dates
Issuance Date
May 13, 2020
Expiry Date
May 13, 2021

