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

MD Atlas
Merz Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Nasenadapter

426058541426058541166043

7 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: 426058541426058541166043
Device name: Nasenadapter
Device model: 74199999
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 21, 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

basicUdiUlid01K82X1CW3PM3PF7GVMK5J98TY

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

7419999904260585411660
7410000204260585410182
7410000004260585410168
7410000104260585410175
7400000604260585410137
7400000804260585410151
7400000704260585410144