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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 Kohlendioxid — 9 UDI-DI variants, MDR

MD Atlas
Nippon Sanso Deutschland GmbH

Data from EUDAMED, last updated May 23, 2026

Medizinisches Kohlendioxid

426021581CO2MEDV8

9 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Nippon Sanso Deutschland GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426021581CO2MEDV8
Device name: Medizinisches Kohlendioxid
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: Nippon Sanso Deutschland GmbH
SRN: DE-MF-000005116
Country: Germany
Email: medgas.germany@eu.nipponsanso.com

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01JKZHQXY6YP6RRYV7K7AMEA7P

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

00183004260215811013
00683004260215811051
00283004260215811037
03083004260215811082
00883004260215811068
01083004260215811075
05083004260215811099
00483004260215811044
Unit of use 1 Liter04260215811020