GUDIDData
eudamed_udi Primary ID: 04052024009459

Bohrdrahtlehre, für Drähte D 1,0 mm - D 2,5 mm (UDI 04052024009459)

Manufactured by INTERCUS GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bohrdrahtlehre, für Drähte D 1,0 mm - D 2,5 mm - Primary ID 04052024009459

Device Regulatory Overview

The Bohrdrahtlehre, für Drähte D 1,0 mm - D 2,5 mm (Model/Catalog Number: 750.105201) is a medical device manufactured by INTERCUS GmbH. This product is indexed under FDA Product Code / Category Classification L091099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
750.105201
Product Code / EMDN
L091099
Device Name
Hilfsmittel zum Längen- und Positionsvergleich
Database Sync Date
2026-08-09 16:45:05

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 Bohrdrahtlehre, für Drähte D 1,0 mm - D 2,5 mm?

The registered manufacturer of record for Bohrdrahtlehre, für Drähte D 1,0 mm - D 2,5 mm is INTERCUS GmbH.

What is the Primary UDI-DI identifier for Bohrdrahtlehre, für Drähte D 1,0 mm - D 2,5 mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04052024009459.

What classification code is assigned to this device?

This device is registered under product classification code L091099.

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