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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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US01 — 2 UDI-DI variants, MDR (UROMED Kurt Drews KG)

MD Atlas
UROMED Kurt Drews KG

Data from EUDAMED, last updated May 31, 2026

US01

04250098810058EZ

2 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

Implantable

Legacy certificates

Certificate number: 20561GB450250724
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: DNV MEDCERT GmbH (0482)
Validity: Jul 24, 2025 → Jul 23, 2030

Identity & classification

Basic UDI-DI: 04250098810058EZ
Device name: US01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Feb 3, 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

basicUdiUlid01KGHZKN76MER5EJPQX5TDWY5B

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 HYDROPUR Ureteral Stent04250098844215
UROMED HYDROPUR Ureteral Stent04250098844246