GUDIDData
eudamed_udi Primary ID: 04250365217742

Klappgriff+ matt gebürstet, 700mm (UDI 04250365217742)

Manufactured by Lehnen GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Klappgriff+ matt gebürstet, 700mm - Primary ID 04250365217742

Device Regulatory Overview

The Klappgriff+ matt gebürstet, 700mm (Model/Catalog Number: L1081004W) is a medical device manufactured by Lehnen GmbH. This product is indexed under FDA Product Code / Category Classification Y181806 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
L1081004W
Product Code / EMDN
Y181806
Device Name
Haltegriff glatt 300mm
Database Sync Date
2026-08-09 16:28:50

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 Klappgriff+ matt gebürstet, 700mm?

The registered manufacturer of record for Klappgriff+ matt gebürstet, 700mm is Lehnen GmbH.

What is the Primary UDI-DI identifier for Klappgriff+ matt gebürstet, 700mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250365217742.

What classification code is assigned to this device?

This device is registered under product classification code Y181806.

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