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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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Trachealkompresse — 43 UDI-DI variants, MDR

MD Atlas
BMV Bender Medical Vertrieb GmbH

Data from EUDAMED, last updated May 23, 2026

Trachealkompresse

4251242611-KompRQ

43 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: 4251242611-KompRQ
Device name: Trachealkompresse
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 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

43 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRXW0X1NYB4CWZZ8DAT8SJDD

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

11302504251242622024
11302104251242600022
11300404251242604709
11300304251242604693
11300204251242604686
11300104251242604679
11303304251242614241
11303904251242600343
11303204251242614234
11301804251242604846
11301304251242604792
11301904251242604853
11301204251242604785
11301704251242604839
11301604251242604822
11301404251242604808
11301504251242600015
11301104251242600008

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