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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Merz Audio — 7 UDI-DI variants, MDR (Merz Medizintechnik GmbH)

MD Atlas
Merz Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Merz Audio

42605854142605854101993W

7 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Merz Medizintechnik GmbH

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Device characteristics

Active deviceMeasuring function

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 42605854142605854101993W
Device name: Merz Audio
Device model: 51050005
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: Merz Medizintechnik GmbH
SRN: DE-MF-000010619
Country: Germany
Email: goldack@merz-medizintechnik.de
Phone: +49 7121 15 98 500

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01K5E991300YN919QKTK8GMZKQ

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

5105001004260585410250
5105001504260585410243
5105002504260585410311
5105002004260585410304
5105000104260585410236
5105003004260585410724
5105000504260585410199