gudid
Primary ID: FX
RGK Octane FX (UDI FX)
Manufactured by RGK WHEELCHAIRS LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RGK Octane FX - Primary ID FX
Device Regulatory Overview
The RGK Octane FX (Model/Catalog Number: FX) is a medical device manufactured by RGK WHEELCHAIRS LIMITED. This product is indexed under FDA Product Code / Category Classification IOR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FX
- Product Code / EMDN
- IOR
- Device Name
- The RGK Octane FX is a made-to-measure chair unlike any other. Imagine a wheelchair that folds down so small you can store it in most airplane overhead luggage compartments. Imagine a wheelchair that is as lightweight and performance-oriented as a rigid sports chair.
- Database Sync Date
- 2026-08-09 09:00:34
Full Regulatory Attributes
🔒 Token Gated
{
"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 RGK Octane FX?
The registered manufacturer of record for RGK Octane FX is RGK WHEELCHAIRS LIMITED.
What is the Primary UDI-DI identifier for RGK Octane FX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FX.
What classification code is assigned to this device?
This device is registered under product classification code IOR.
Similar Classification Devices (IOR)
Other Devices by RGK WHEELCHAIRS LIMITED
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