GUDIDData
eudamed_udi Primary ID: 00840363371207

Axiom (UDI 00840363371207)

Manufactured by Ki Mobility LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Axiom - Primary ID 00840363371207

Device Regulatory Overview

The Axiom (Model/Catalog Number: XSP1720VIC) is a medical device manufactured by Ki Mobility LLC. This product is indexed under FDA Product Code / Category Classification V080399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
XSP1720VIC
Product Code / EMDN
V080399
Device Name
Seating
Database Sync Date
2026-08-09 16:28:59

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Axiom?

The registered manufacturer of record for Axiom is Ki Mobility LLC.

What is the Primary UDI-DI identifier for Axiom?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840363371207.

What classification code is assigned to this device?

This device is registered under product classification code V080399.

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