gudid
Primary ID: CE
Inogen At Home Stationary Concentrator (UDI CE)
Manufactured by Inogen, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Inogen At Home Stationary Concentrator - Primary ID CE
Device Regulatory Overview
The Inogen At Home Stationary Concentrator (Model/Catalog Number: CE) 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
- CE
- Product Code / EMDN
- CAW
- Device Name
- Inogen At Home Stationary Concentrator, CE (10-06316-XX-XX)
- Database Sync Date
- 2026-08-09 09:31:22
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Inogen At Home Stationary Concentrator?
The registered manufacturer of record for Inogen At Home Stationary Concentrator is Inogen, Inc..
What is the Primary UDI-DI identifier for Inogen At Home Stationary Concentrator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CE.
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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint