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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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Sauerstoff-Sicherheitsschlauch — 2 UDI-DI variants, MDR

MD Atlas
BMV Bender Medical Vertrieb GmbH

Data from EUDAMED, last updated May 23, 2026

Sauerstoff-Sicherheitsschlauch

4251242613-61QN

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: BMV Bender Medical Vertrieb GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4251242613-61QN
Device name: Sauerstoff-Sicherheitsschlauch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 14, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01KRK86XBF8GN36WVNRXR9YFF2

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

13610204251242607441
13610304251242607458