GUDIDData
eudamed_udi Primary ID: 1311813WG305X610RF113

Winkelgriff 90°, 305 x 610 mm, Rechts (UDI 1311813WG305X610RF113)

Manufactured by FRELU GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Winkelgriff 90°, 305 x 610 mm, Rechts - Primary ID 1311813WG305X610RF113

Device Regulatory Overview

The Winkelgriff 90°, 305 x 610 mm, Rechts (Model/Catalog Number: WG305X610RF) 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
WG305X610RF
Product Code / EMDN
Y181803
Device Name
Haltegriffe
Database Sync Date
2026-08-09 17:23:03

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 Winkelgriff 90°, 305 x 610 mm, Rechts?

The registered manufacturer of record for Winkelgriff 90°, 305 x 610 mm, Rechts is FRELU GmbH.

What is the Primary UDI-DI identifier for Winkelgriff 90°, 305 x 610 mm, Rechts?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1311813WG305X610RF113.

What classification code is assigned to this device?

This device is registered under product classification code Y181803.

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