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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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Q Path NovaBrush — 7 UDI-DI variants, MDR (VWR INTERNATIONAL SAS)

MD Atlas
VWR INTERNATIONAL SAS

Data from EUDAMED, last updated May 19, 2026

Q Path NovaBrush

731205U001AF

7 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: VWR INTERNATIONAL SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 731205U001AF
Device name: Q Path NovaBrush
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: VWR INTERNATIONAL SAS
SRN: FR-MF-000016509
Country: France
Email: fr.regulatoryaffairs@avantorsciences.com

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KAV7EH5723E6KHKJKEZ5ZEGS

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

Q Path NovaBrush 1 undetachable07312056604983
Q Path NovaBrush 207312056605034
Q Path NovaBrush 207312056605003
Q Path NovaBrush 2 undetachable07312056605065
Q Path NovaBrush 307312056605089
Q Path NovaBrush 307312056605119
Q Path NovaBrush 4 undetachable07312056591672