gudid
Primary ID: SIMEOX
SIMEOX (UDI SIMEOX)
Manufactured by Inogen, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SIMEOX - Primary ID SIMEOX
Device Regulatory Overview
The SIMEOX (Model/Catalog Number: SIMEOX) is a medical device manufactured by Inogen, Inc.. This product is indexed under FDA Product Code / Category Classification SDT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SIMEOX
- Product Code / EMDN
- SDT
- Device Name
- Simeox_H airway clearance device, with remote control, power supply, transport bag and user manual
- Database Sync Date
- 2026-08-09 09:59:20
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 SIMEOX?
The registered manufacturer of record for SIMEOX is Inogen, Inc..
What is the Primary UDI-DI identifier for SIMEOX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SIMEOX.
What classification code is assigned to this device?
This device is registered under product classification code SDT.
Similar Classification Devices (SDT)
Other Devices by Inogen, Inc.
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