GUDIDData
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eudamed_udi Primary ID: 04052024054664

GNp T-Griff modular (UDI 04052024054664)

Manufactured by INTERCUS GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GNp T-Griff modular - Primary ID 04052024054664

Device Regulatory Overview

The GNp T-Griff modular (Model/Catalog Number: 1133151) is a medical device manufactured by INTERCUS GmbH. This product is indexed under FDA Product Code / Category Classification L99 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1133151
Product Code / EMDN
L99
Device Name
Instrumente für GN Gleitnagelsystem (nicht invasiv)
Database Sync Date
2026-08-09 16:29:30

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 GNp T-Griff modular?

The registered manufacturer of record for GNp T-Griff modular is INTERCUS GmbH.

What is the Primary UDI-DI identifier for GNp T-Griff modular?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04052024054664.

What classification code is assigned to this device?

This device is registered under product classification code L99.

Similar Classification Devices (L99)

Other Devices by INTERCUS GmbH

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