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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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ERCP-Katheter — 2 UDI-DI variants, MDR (MTW - Endoskopie W. Haag KG)

MD Atlas
MTW - Endoskopie W. Haag KG

Data from EUDAMED, last updated May 23, 2026

ERCP-Katheter

4046223G0304010103ASXXXVP

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: MTW - Endoskopie W. Haag KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4046223G0304010103ASXXXVP
Device name: ERCP-Katheter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 12, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01KRDGC6VA53G1PXDYVE20KK83

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

99013020004046223009679
99013020204046223043505