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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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Medical Liquid Nitrogen — 3 UDI-DI variants, MDR

MD Atlas
Air Liquide Medical sa

Data from EUDAMED, last updated May 23, 2026

Medical Liquid Nitrogen

5430003250LIN-DERMATOSV

3 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: Air Liquide Medical sa

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Device characteristics

Active device

Legacy certificates

Certificate number: MDR 00102-A
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: KIWA CERMET ITALIA S.P.A. (0476)
Validity: May 12, 2025 → May 11, 2030

Identity & classification

Basic UDI-DI: 5430003250LIN-DERMATOSV
Device name: Medical Liquid Nitrogen
Device model: Medical Liquid Nitrogen for Dermatology
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: Air Liquide Medical sa
SRN: BE-MF-000022114
Country: Belgium
Email: sales.almbenelux@airliquide.com
Phone: +32 (0)2 431 73 00

Variants by status

UDI-DI variants

3 UDI-DI variants

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basicUdiUlid01KJWWAFSDQCECYKJSEDAPNA9A

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

M4125RG05430003250082
M4100R18RMA00105430003250068
M4100R45RMA00105430003250075