GUDIDData
eudamed_udi Primary ID: 1311813RLK-760X1140VG106

Duschhandlauf 760 x 1.140 mm, glatt, verdeckte Montage (UDI 1311813RLK-760X1140VG106)

Manufactured by FRELU GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Duschhandlauf 760 x 1.140 mm, glatt, verdeckte Montage - Primary ID 1311813RLK-760X1140VG106

Device Regulatory Overview

The Duschhandlauf 760 x 1.140 mm, glatt, verdeckte Montage (Model/Catalog Number: RLK-760X1140VG) is a medical device manufactured by FRELU GmbH. This product is indexed under FDA Product Code / Category Classification Y181803 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
RLK-760X1140VG
Product Code / EMDN
Y181803
Device Name
Haltegriffe
Database Sync Date
2026-08-09 16:29:08

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 Duschhandlauf 760 x 1.140 mm, glatt, verdeckte Montage?

The registered manufacturer of record for Duschhandlauf 760 x 1.140 mm, glatt, verdeckte Montage is FRELU GmbH.

What is the Primary UDI-DI identifier for Duschhandlauf 760 x 1.140 mm, glatt, verdeckte Montage?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1311813RLK-760X1140VG106.

What classification code is assigned to this device?

This device is registered under product classification code Y181803.

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