GUDIDData
eudamed_udi Primary ID: 04260203793888

Kryo-Set max | weiß (UDI 04260203793888)

Manufactured by Novafon Elektromedizinische Geräte GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kryo-Set max | weiß - Primary ID 04260203793888

Device Regulatory Overview

The Kryo-Set max | weiß (Model/Catalog Number: 7114-040) is a medical device manufactured by Novafon Elektromedizinische Geräte GmbH. This product is indexed under FDA Product Code / Category Classification Z120612 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
7114-040
Product Code / EMDN
Z120612
Device Name
Kryo-Set
Database Sync Date
2026-08-09 17:51:31

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 Kryo-Set max | weiß?

The registered manufacturer of record for Kryo-Set max | weiß is Novafon Elektromedizinische Geräte GmbH.

What is the Primary UDI-DI identifier for Kryo-Set max | weiß?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260203793888.

What classification code is assigned to this device?

This device is registered under product classification code Z120612.

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