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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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AIRO ANTISNORING — 4 UDI-DI variants, MDR (QReverse Srl)

MD Atlas
QReverse Srl

Data from EUDAMED, last updated May 31, 2026

AIRO ANTISNORING

805259043AIROBT

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: QReverse Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805259043AIROBT
Device name: AIRO ANTISNORING
Device model: QRS.P.0.000.00.A
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: QReverse Srl
SRN: IT-MF-000052072
Country: Italy
Email: giuliano.m@qreverse.it

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KH69FVRA2ZBY3KCH93P5Y9CN

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

QRS.P.0.000.00.A08052590430004
QRS.P.0.003.00.A08052590430035
QRS.P.0.002.00.A08052590430028
QRS.P.0.001.00.A08052590430011