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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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Ohrstöpsel — 60 UDI-DI variants, MDR (Merz Medizintechnik GmbH)

MD Atlas
Merz Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Ohrstöpsel

426058541426058541165346

60 UDI-DI variants

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426058541426058541165346
Device name: Ohrstöpsel
Device model: 75999999
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 19, 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

60 UDI-DI variants

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Applied filters

basicUdiUlid01K5GA3G3Q2TGR47TWQZ7P9HY6

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

7300008604260585411103
7300009004260585411141
7300008204260585411066
7300008504260585411097
7300008904260585411134
7300008104260585411059
7300009204260585411165
7300009304260585411172
7300008704260585411110
7300008304260585411073

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