GUDIDData
eudamed_udi Primary ID: 04052024043422

Lagerungssieb, für PENTA-Platten, polyaxial, Kleinfragment (UDI 04052024043422)

Manufactured by INTERCUS GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lagerungssieb, für PENTA-Platten, polyaxial, Kleinfragment - Primary ID 04052024043422

Device Regulatory Overview

The Lagerungssieb, für PENTA-Platten, polyaxial, Kleinfragment (Model/Catalog Number: 750.108024) is a medical device manufactured by INTERCUS GmbH. This product is indexed under FDA Product Code / Category Classification V0480 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
750.108024
Product Code / EMDN
V0480
Device Name
Lagerungssysteme für Implantate und Instrumente (Kunststoff / Metall)
Database Sync Date
2026-08-09 16:58:57

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 Lagerungssieb, für PENTA-Platten, polyaxial, Kleinfragment?

The registered manufacturer of record for Lagerungssieb, für PENTA-Platten, polyaxial, Kleinfragment is INTERCUS GmbH.

What is the Primary UDI-DI identifier for Lagerungssieb, für PENTA-Platten, polyaxial, Kleinfragment?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04052024043422.

What classification code is assigned to this device?

This device is registered under product classification code V0480.

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