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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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Nebula — 11 UDI-DI variants, MDR (Air Liquide Medical Systems S.r.l.)

MD Atlas
Air Liquide Medical Systems S.r.l.

Data from EUDAMED, last updated May 31, 2026

Nebula

8015662NEBULATB

11 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 Systems S.r.l.

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 8015662NEBULATB
Device name: Nebula
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: Air Liquide Medical Systems S.r.l.
SRN: IT-MF-000015627
Country: Italy
Email: gianluigi.brembilla@airliquide.com
Phone: +39 0302015911

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP8NJBYB729W92KW7SCV05FB

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

40113108015662011310
40120008015662012003
40118708015662011877
40116808015662011686
40116208015662011624
40112408015662011242
40112308015662011235
40116008015662011600
40116408015662011648
40116108015662011617
40118208015662011822