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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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Medizinisches Gasleitungssystem — 5 UDI-DI variants, MDR

MD Atlas
Heyer Aerotech GmbH

Data from EUDAMED, last updated May 23, 2026

Medizinisches Gasleitungssystem

425560390NV

5 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Heyer Aerotech GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 425560390NV
Device name: Medizinisches Gasleitungssystem
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Heyer Aerotech GmbH
SRN: DE-MF-000013791
Country: Germany
Email: joana.mueller@heyer-aerotech.de
Phone: +49 2603 5070743

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KM5ETCBMEJAAY3ZJS92G8R6R

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

537321604255603950153
537322004255603950177
536332004255603950092
537332004255603950214
537321904255603950160