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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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Kanülenreinigungsbürste — 15 UDI-DI variants, MDR

MD Atlas
BMV Bender Medical Vertrieb GmbH

Data from EUDAMED, last updated May 23, 2026

Kanülenreinigungsbürste

4251242612-20PZ

15 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: BMV Bender Medical Vertrieb GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4251242612-20PZ
Device name: Kanülenreinigungsbürste
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: BMV Bender Medical Vertrieb GmbH
SRN: DE-MF-000005283
Country: Germany
Email: info@bmv-med.de
Phone: +49 2245 610 940

Variants by status

UDI-DI variants

15 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRP0Y8CYK6HYB37ZD7MSYCY1

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

122010-10 04251242605300
122010-12 04251242605317
122010-14 04251242605324
122010-04 04251242605270
122010-06 04251242605287
122010-08 04251242605294
122030-1004251242600381
122030-0604251242600398
122030-0804251242600374
122020-10 04251242605379
122020-12 04251242605386
122020-14 04251242605393
122020-04 04251242605348
122020-06 04251242605355
122020-08 04251242605362