Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

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

7599999904260585411653
7300006204260585411233
7150008104260585411318
7150008504260585411356
7150007704260585411257
7150007904260585411295
7150008304260585411332
7150007504260585411271
7150009104260585411387
7150008204260585411325
7150007404260585411288
7150007804260585411240
7150008004260585411301
7150008404260585411349
7150008904260585411363
7150007604260585411264
7150009004260585411370
7150006504260585411202
7150006604260585411219
7150006304260585411189
7150006404260585411196
7150006704260585411226
7300002904260585410960
7300002504260585410922
7300002704260585410946

1 2 3