eudamed_udi Primary ID: 08053470214073

Unspecified Brand (UDI 08053470214073)

Manufactured by GE.ME.S. GENERAL MEDICAL SUPPLIES S.R.L.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: TRA.2024S) is a medical device manufactured by GE.ME.S. GENERAL MEDICAL SUPPLIES S.R.L.. This product is indexed under FDA Product Code / Category Classification P09120602 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: TRA.2024S
Product Code / EMDN: P09120602
Device Name: Cancellous Osteosynthesis 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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is GE.ME.S. GENERAL MEDICAL SUPPLIES S.R.L..

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053470214073.

What classification code is assigned to this device?

This device is registered under product classification code P09120602.

Similar Classification Devices (P09120602)

Other Devices by GE.ME.S. GENERAL MEDICAL SUPPLIES S.R.L.

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