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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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TBC03 — 4 UDI-DI variants, MDR (UROMED Kurt Drews KG)

MD Atlas
UROMED Kurt Drews KG

Data from EUDAMED, last updated May 23, 2026

TBC03

04250098810033EH

4 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: 04250098810033EH
Device name: TBC03
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

4 UDI-DI variants

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Applied filters

basicUdiUlid01KGHK7HDMKTWK1BDE9A7PYQX8

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 PROSIL Transurethral Silicone Balloon Catheter for Children04250098821421
UROMED PROSIL Transurethral Silicone Balloon Catheter for Children04250098821452
UROMED PROSIL Transurethral Silicone Balloon Catheter for Children04250098821391
UROMED SILUCENT Transurethral Silicone Balloon Catheter04250098848749