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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 Hospital F Non Vented… — 3 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 31, 2026

Respireo Hospital F Non Vented Disposable

8015662RESPHOSPFNVDAV

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 Systems S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8015662RESPHOSPFNVDAV
Device name: Respireo Hospital F Non Vented Disposable
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 4, 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

3 UDI-DI variants

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Applied filters

basicUdiUlid01K97N5N9XS23DWTD7FAV2RCB7

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

47254308015662725439
47254208015662725422
47254408015662725446