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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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QualiBreath — 13 UDI-DI variants, MDR (Qualiteam s.r.l.)

MD Atlas
Qualiteam s.r.l.

Data from EUDAMED, last updated May 30, 2026

QualiBreath

803367519QB00B9

13 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: Qualiteam s.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803367519QB00B9
Device name: QualiBreath
Device model: QualiBreath
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: Qualiteam s.r.l.
SRN: IT-MF-000026616
Country: Italy
Email: info@qualiteam.com

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01KRBMXW4ZGRY7XY3J5J85VTW5

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

QB-4XL08033675190167
QB-5XL08033675199917
QB-L08033675190044
QB-M08033675190037
QB-S08033675190020
QB-XL08033675190051
QB-XS08033675190013
QB-XXL08033675190068
QB-XXXL08033675190075
QB TOD108033675190488
QB-INF3508033675190945
QB-INF3008033675190914
QB TOD208033675190495