gudid
Primary ID: 1425-1001
OxyGo Adult Cannula (UDI 1425-1001)
Manufactured by WESTMED, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OxyGo Adult Cannula - Primary ID 1425-1001
Device Regulatory Overview
The OxyGo Adult Cannula (Model/Catalog Number: 1425-1001) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification CAT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1425-1001
- Product Code / EMDN
- CAT
- Device Name
- Length- 7'
- Database Sync Date
- 2026-08-09 09:04:13
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of OxyGo Adult Cannula?
The registered manufacturer of record for OxyGo Adult Cannula is WESTMED, INC..
What is the Primary UDI-DI identifier for OxyGo Adult Cannula?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1425-1001.
What classification code is assigned to this device?
This device is registered under product classification code CAT.
Similar Classification Devices (CAT)
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