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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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Provox TubeBrush — 2 UDI-DI variants, MDR (Atos Medical AB)

MD Atlas
Atos Medical AB

Data from EUDAMED, last updated May 31, 2026

Provox TubeBrush

7331791-GEN-A-000-0001-E9

2 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: Atos Medical AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7331791-GEN-A-000-0001-E9
Device name: Provox TubeBrush
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Atos Medical AB
SRN: SE-MF-000000725
Country: Sweden
Email: info@atosmedical.com
Phone: +4641519800

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KMQCX2WRXQZM0E3CJBQ0VSDA

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

766107331791002663
766007331791002656