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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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GI03 — 2 UDI-DI variants, MDR (UROMED Kurt Drews KG)

MD Atlas
UROMED Kurt Drews KG

Data from EUDAMED, last updated May 23, 2026

GI03

04250098810053EP

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: UROMED Kurt Drews KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 04250098810053EP
Device name: GI03
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: UROMED Kurt Drews KG
SRN: DE-MF-000006084
Country: Germany
Email: service@uromed.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KEEQ1ET0NFWEJ3RDFJAF6S5H

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

UROMED Guide Wire »Lunderquist ASP«04250098805681
UROMED Guide Wire »Lunderquist ASP«04250098805650