GUDIDData
eudamed_udi Primary ID: 04250485300256

GUILEN Saug Raspatorium mit Mandrin nach rechts gebogen 20 cm lang (UDI 04250485300256)

Manufactured by Zepf Medical Instruments GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GUILEN Saug Raspatorium mit Mandrin nach rechts gebogen 20 cm lang - Primary ID 04250485300256

Device Regulatory Overview

The GUILEN Saug Raspatorium mit Mandrin nach rechts gebogen 20 cm lang (Model/Catalog Number: 46-6509-20) is a medical device manufactured by Zepf Medical Instruments GmbH. This product is indexed under FDA Product Code / Category Classification L030199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
46-6509-20
Product Code / EMDN
L030199
Device Name
Schaber
Database Sync Date
2026-08-09 16:29:04

Full Regulatory Attributes

๐Ÿ”’ 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 GUILEN Saug Raspatorium mit Mandrin nach rechts gebogen 20 cm lang?

The registered manufacturer of record for GUILEN Saug Raspatorium mit Mandrin nach rechts gebogen 20 cm lang is Zepf Medical Instruments GmbH.

What is the Primary UDI-DI identifier for GUILEN Saug Raspatorium mit Mandrin nach rechts gebogen 20 cm lang?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250485300256.

What classification code is assigned to this device?

This device is registered under product classification code L030199.

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