KENXIN OXYGEN MASK WITH TUBE (ADULT) - FDA Registration DVR-6419
Access comprehensive regulatory information for KENXIN OXYGEN MASK WITH TUBE (ADULT) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-6419 and manufactured by Kenxin International Company Ltd. in China. The device was registered on May 09, 2019.
This page provides complete registration details including manufacturer information, importer/distributor details (Indoplas 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.
Free Database
Powered by Pure Global AI
FDA Official Data
China
DVR-6419
KENXIN OXYGEN MASK WITH TUBE (ADULT)
Registered medical device in Philippines
Device Information
Product Name
KENXIN OXYGEN MASK WITH TUBE (ADULT)
Registration Number
DVR-6419
Manufacturer Details
Manufacturer
Kenxin International Company Ltd.Country of Origin
China
Importer & Distribution
Importer/Distributor
Indoplas Philippines, Inc.Registration Dates
Issuance Date
May 09, 2019
Expiry Date
January 30, 2024

