eudamed_udi Primary ID: 07640140832623

Guichet Screw (UDI 07640140832623)

Manufactured by X-os S.A.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Guichet Screw (Model/Catalog Number: GSC5585) 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: GSC5585
Product Code / EMDN: P09120604
Device Name: Guichet Screw
Database Sync Date: 2026-08-09 16:29:38

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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Frequently Asked Questions

Who is the primary manufacturer of Guichet Screw?

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

What is the Primary UDI-DI identifier for Guichet Screw?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640140832623.

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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