gudid
Primary ID: 630
OxyGo Fit (UDI 630)
Manufactured by Inogen, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OxyGo Fit - Primary ID 630
Device Regulatory Overview
The OxyGo Fit (Model/Catalog Number: 630) 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
- 630
- Product Code / EMDN
- CAW
- Device Name
- OxyGo Fit (Inogen One G4 Oxygen Concentrator) (10-07068-XX-XX) (1400-2000)
- 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 Fit?
The registered manufacturer of record for OxyGo Fit is Inogen, Inc..
What is the Primary UDI-DI identifier for OxyGo Fit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 630.
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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