GUDIDData
eudamed_udi Primary ID: 04260585410250

audioboX 12 Kanäle (UDI 04260585410250)

Manufactured by Merz Medizintechnik GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for audioboX 12 Kanäle - Primary ID 04260585410250

Device Regulatory Overview

The audioboX 12 Kanäle (Model/Catalog Number: 51050010) is a medical device manufactured by Merz Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification Z121401 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
51050010
Product Code / EMDN
Z121401
Device Name
Merz Audio
Database Sync Date
2026-08-09 17:12:25

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 audioboX 12 Kanäle?

The registered manufacturer of record for audioboX 12 Kanäle is Merz Medizintechnik GmbH.

What is the Primary UDI-DI identifier for audioboX 12 Kanäle?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260585410250.

What classification code is assigned to this device?

This device is registered under product classification code Z121401.

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