GUDIDData
eudamed_udi Primary ID: 04250379938558

Exkavator 8kant Fig. 28 (UDI 04250379938558)

Manufactured by Zepf Medical Instruments GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Exkavator 8kant Fig. 28 - Primary ID 04250379938558

Device Regulatory Overview

The Exkavator 8kant Fig. 28 (Model/Catalog Number: 83-4405-28) is a medical device manufactured by Zepf Medical Instruments GmbH. This product is indexed under FDA Product Code / Category Classification L159002 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
83-4405-28
Product Code / EMDN
L159002
Device Name
Exkavator, dental
Database Sync Date
2026-08-09 16:30:07

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 Exkavator 8kant Fig. 28?

The registered manufacturer of record for Exkavator 8kant Fig. 28 is Zepf Medical Instruments GmbH.

What is the Primary UDI-DI identifier for Exkavator 8kant Fig. 28?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250379938558.

What classification code is assigned to this device?

This device is registered under product classification code L159002.

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