gudid
Primary ID: 840
OxyGo (UDI 840)
Manufactured by Inogen, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OxyGo - Primary ID 840
Device Regulatory Overview
The OxyGo (Model/Catalog Number: 840) is a medical device manufactured by Inogen, Inc.. This product is indexed under FDA Product Code / Category Classification CAW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 840
- Product Code / EMDN
- CAW
- Device Name
- OxyGo (Inogen One G3 Oxygen Concentrator) (10-05560-XX-XX) (1400-1000)
- Database Sync Date
- 2026-08-09 09:31:22
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?
The registered manufacturer of record for OxyGo is Inogen, Inc..
What is the Primary UDI-DI identifier for OxyGo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 840.
What classification code is assigned to this device?
This device is registered under product classification code CAW.
Similar Classification Devices (CAW)
Other Devices by Inogen, Inc.
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