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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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ISC01 — 8 UDI-DI variants, MDR (UROMED Kurt Drews KG)

MD Atlas
UROMED Kurt Drews KG

Data from EUDAMED, last updated May 23, 2026

ISC01

04250098810019EP

8 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: UROMED Kurt Drews KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 04250098810019EP
Device name: ISC01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 27, 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

8 UDI-DI variants

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Applied filters

basicUdiUlid01KG0B1X685PHXA897K0T3WKPR

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 SIMPLYCATH mobil Trial Set »male«04250098835763
UROMED SIMPLYCATH mobil Trial Set »male«04250098835756
UROMED SIMPLYCATH mobil Trial Set »male«04250098835770
UROMED SIMPLYCATH mobil Trial Set »male«04250098835787
UROMED SIMPLYCATH mobil Trial Set »pouch«04250098835824
UROMED SIMPLYCATH mobil Trial Set »pouch«04250098835855
UROMED SIMPLYCATH mobil Trial Set »pouch«04250098835831
UROMED SIMPLYCATH mobil Trial Set »pouch«04250098835848