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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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Fixierung für Nasotrachealtuben — 4 UDI-DI variants, MDR

MD Atlas
Novo Klinik-Service GmbH

Data from EUDAMED, last updated May 23, 2026

Fixierung für Nasotrachealtuben

426040264V190Z4

4 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: Novo Klinik-Service GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426040264V190Z4
Device name: —
Device model: Fixierung für Nasotrachealtuben
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: Novo Klinik-Service GmbH
SRN: DE-MF-000005289
Country: Germany
Email: info@novo-med.de

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KAXK89M7P9XSPEVWB60EMC2X

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

N1952201004260402646107
805 60104260402646190
N1952001004260402646091
805 50104260402646183