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eudamed_udi Primary ID: 07640140833866

Guichet Femur V2 (UDI 07640140833866)

Manufactured by X-os S.A.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Guichet Femur V2 - Primary ID 07640140833866

Device Regulatory Overview

The Guichet Femur V2 (Model/Catalog Number: GF21128NS) is a medical device manufactured by X-os S.A.. This product is indexed under FDA Product Code / Category Classification P09120604 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
GF21128NS
Product Code / EMDN
P09120604
Device Name
Guichet Lengthening Nail System
Database Sync Date
2026-08-09 16:28:55

Full Regulatory Attributes

đź”’ 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 Guichet Femur V2?

The registered manufacturer of record for Guichet Femur V2 is X-os S.A..

What is the Primary UDI-DI identifier for Guichet Femur V2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640140833866.

What classification code is assigned to this device?

This device is registered under product classification code P09120604.

Similar Classification Devices (P09120604)

Other Devices by X-os S.A.

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