GUDIDData
eudamed_udi Primary ID: 1311813HLK-770X770VG162

Duschhandlauf 770 x 770 mm, glatt, verdeckte Montage (UDI 1311813HLK-770X770VG162)

Manufactured by FRELU GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Duschhandlauf 770 x 770 mm, glatt, verdeckte Montage - Primary ID 1311813HLK-770X770VG162

Device Regulatory Overview

The Duschhandlauf 770 x 770 mm, glatt, verdeckte Montage (Model/Catalog Number: HLK-770X770VG) 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
HLK-770X770VG
Product Code / EMDN
Y181803
Device Name
Haltegriffe
Database Sync Date
2026-08-09 17:59:54

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Duschhandlauf 770 x 770 mm, glatt, verdeckte Montage?

The registered manufacturer of record for Duschhandlauf 770 x 770 mm, glatt, verdeckte Montage is FRELU GmbH.

What is the Primary UDI-DI identifier for Duschhandlauf 770 x 770 mm, glatt, verdeckte Montage?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1311813HLK-770X770VG162.

What classification code is assigned to this device?

This device is registered under product classification code Y181803.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint