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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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Synthetische Luft-Medizinprodukt — 11 UDI-DI variants, MDR

MD Atlas
Messer Industriegase GmbH

Data from EUDAMED, last updated May 23, 2026

Synthetische Luft-Medizinprodukt

426238912MIGG018M

11 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: Messer Industriegase GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426238912MIGG018M
Device name: Synthetische Luft-Medizinprodukt
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 11, 2022

Manufacturer & authorised representative

Manufacturer

Name: Messer Industriegase GmbH
SRN: DE-MF-000016610
Country: Germany
Email: info.de@messergroup.com

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GF3P7VJAQ2399T2Q7WE03750

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

MIGG0104262389120007
10018205204262389120045
30018250204262389120090
30018205204262389120052
30018210204262389120076
30018202204262389120014
10018203204262389120021
10018210204262389120069
100182502 04262389120083
30018220204262389120519
30018203204262389120038