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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 — 4 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

4046223G0304010101ASJXXSP

4 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: 4046223G0304010101ASJXXSP
Device name: ERCP-Katheter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 8, 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

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR3HXTJ4217N7FX7R7VBVHHG

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

99013111104046223030147
99013013204046223046612
99013011204046223043543
9913013111004046223040795