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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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Terminal Unit — 7 UDI-DI variants, MDR

MD Atlas
Air Liquide Medical Systems S.A.

Data from EUDAMED, last updated May 19, 2026

Terminal Unit

37005043BM_TERM_UNIT3W

7 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37005043BM_TERM_UNIT3W
Device name: Terminal Unit
Device model: Terminal Unit NF
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Feb 13, 2026

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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KHBGYMR44KVGWR67YVM4F4XP

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

Terminal unit BM NF Air03700504301456
Terminal unit BM NF Air-80003700504301531
Terminal unit BM NF CO203700504301517
Terminal unit BM NF N2-80003700504301494
Terminal unit BM NF N2O03700504301470
Terminal Unit BM NF O203700504301418
Terminal unit BM NF VAC03700504301432