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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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Führungskatheter — 3 UDI-DI variants, MDR

MD Atlas
MTW - Endoskopie W. Haag KG

Data from EUDAMED, last updated May 23, 2026

Führungskatheter

4046223P058001XXXXFBPGH5D

3 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: MTW - Endoskopie W. Haag KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4046223P058001XXXXFBPGH5D
Device name: Führungskatheter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: MTW - Endoskopie W. Haag KG
SRN: DE-MF-000004993
Country: Germany
Email: info@mtw-endoskopie.com
Phone: +49 2803 9120 0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KR0H7YC6S5Q5DAW579N8B2NR

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

041081604046223051890
041181604046223051920
040981604046223051869