GUDIDData
eudamed_udi Primary ID: 04250379944160

Abdr.Löffel gel.C1/2-3 rechts (UDI 04250379944160)

Manufactured by Zepf Medical Instruments GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Abdr.Löffel gel.C1/2-3 rechts - Primary ID 04250379944160

Device Regulatory Overview

The Abdr.Löffel gel.C1/2-3 rechts (Model/Catalog Number: 86-1501-03) is a medical device manufactured by Zepf Medical Instruments GmbH. This product is indexed under FDA Product Code / Category Classification Q010503 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
86-1501-03
Product Code / EMDN
Q010503
Device Name
Abdruckform, dental
Database Sync Date
2026-08-09 16:29:28

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 Abdr.Löffel gel.C1/2-3 rechts?

The registered manufacturer of record for Abdr.Löffel gel.C1/2-3 rechts is Zepf Medical Instruments GmbH.

What is the Primary UDI-DI identifier for Abdr.Löffel gel.C1/2-3 rechts?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250379944160.

What classification code is assigned to this device?

This device is registered under product classification code Q010503.

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