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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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XO / XO SMART — 9 UDI-DI variants, MDR

MD Atlas
Air Liquide Medical Systems S.A.

Data from EUDAMED, last updated May 19, 2026

XO / XO SMART

37005043XO7A

9 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: Air Liquide Medical Systems S.A.

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 37005043XO7A
Device name: XO / XO SMART
Device model: XO / XO SMART
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jun 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: Air Liquide Medical Systems S.A.
SRN: FR-MF-000003649
Country: France
Email: DL-FR-alms-affaires-reglementaires@airliquide.com

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JY1EDXN81XXQC5S9PMPXVBJV

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

CK06253903700504301104
CK06253803700504301081
CK06254103700504301142
CK06254003700504301128
CK06254903700504301180
CK06254803700504301166
CK06255103700504301227
CK06255003700504301203
CK06255403700504301302