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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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SCS01 — 14 UDI-DI variants, MDR (UROMED Kurt Drews KG)

MD Atlas
UROMED Kurt Drews KG

Data from EUDAMED, last updated May 23, 2026

SCS01

04250098810078F7

14 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: UROMED Kurt Drews KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 04250098810078F7
Device name: SCS01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Feb 9, 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

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KH0NV8TZNCYBRTA4H84PMTZP

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

3031.1204250098846134
3031.1404250098846165
UROMED Suprapubic Exchange Set04250098807456
UROMED Suprapubic Exchange Set04250098807487
UROMED Suprapubic Exchange Set04250098807425
3015.1204250098807210
3021.1204250098807272
3046.1404250098807692
3026.1404250098807333
3046.1204250098807661
3027.1804250098814324
3046.1604250098807722
3027.2004250098814355
3027.1604250098807364