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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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Respireo SOFT Nasal — 7 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 30, 2026

Respireo SOFT Nasal

8015662RESPSOFTNVZ

7 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8015662RESPSOFTNVZ
Device name: Respireo SOFT Nasal
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 18, 2025

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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KABJGB2QB9N0WZ1634ZQ6S4C

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

47236008015662723602
47233708015662723374
47235808015662723589
47233808015662723381
47236108015662723619
47235308015662723534
47235208015662723527