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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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ISC02 — 10 UDI-DI variants, MDR (UROMED Kurt Drews KG)

MD Atlas
UROMED Kurt Drews KG

Data from EUDAMED, last updated May 23, 2026

ISC02

04250098810015EF

10 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: 04250098810015EF
Device name: ISC02
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

10 UDI-DI variants

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Applied filters

basicUdiUlid01KG08Z4827NEJ5JSPXYYYB9KJ

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

3600.1804250098820028
3600.1004250098819909
3610.0804250098820295
3610.1204250098820356
3600.1204250098819930
3600.1604250098819992
3610.1604250098820417
3600.1404250098819961
3610.1004250098820325
3610.1404250098820387