GUDIDData
eudamed_udi Primary ID: 04250485320940

Knochenhebel 22 mm 24 cm 90º (UDI 04250485320940)

Manufactured by Zepf Medical Instruments GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Knochenhebel 22 mm 24 cm 90º - Primary ID 04250485320940

Device Regulatory Overview

The Knochenhebel 22 mm 24 cm 90º (Model/Catalog Number: 32-7936-22) is a medical device manufactured by Zepf Medical Instruments GmbH. This product is indexed under FDA Product Code / Category Classification L0902 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
32-7936-22
Product Code / EMDN
L0902
Device Name
Elevatorium, Orthopädie
Database Sync Date
2026-08-09 16:46:00

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 Knochenhebel 22 mm 24 cm 90º?

The registered manufacturer of record for Knochenhebel 22 mm 24 cm 90º is Zepf Medical Instruments GmbH.

What is the Primary UDI-DI identifier for Knochenhebel 22 mm 24 cm 90º?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250485320940.

What classification code is assigned to this device?

This device is registered under product classification code L0902.

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