eudamed_udi Primary ID: 04008244509552

Handlauf (UDI 04008244509552)

Manufactured by RUD Ketten Rieger & Dietz GmbH u. Co. KG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Handlauf (Model/Catalog Number: 5581503) is a medical device manufactured by RUD Ketten Rieger & Dietz GmbH u. Co. KG. This product is indexed under FDA Product Code / Category Classification Y181803 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 5581503
Product Code / EMDN: Y181803
Device Name: Handläufe
Database Sync Date: 2026-08-09 16:44:55

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 Handlauf?

The registered manufacturer of record for Handlauf is RUD Ketten Rieger & Dietz GmbH u. Co. KG.

What is the Primary UDI-DI identifier for Handlauf?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04008244509552.

What classification code is assigned to this device?

This device is registered under product classification code Y181803.

Similar Classification Devices (Y181803)

Other Devices by RUD Ketten Rieger & Dietz GmbH u. Co. KG

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