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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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RÜSCH Bladder Catheter Tiemann — 7 UDI-DI variants, MDR

MD Atlas
Teleflex Medical

Data from EUDAMED, last updated May 24, 2026

RÜSCH Bladder Catheter Tiemann

08019020000000000000170KJ

7 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: Teleflex Medical

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 08019020000000000000170KJ
Device name: RÜSCH Bladder Catheter Tiemann
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: Teleflex Medical
SRN: IE-MF-000015868
Country: Ireland
Email: orders.intl@teleflex.com
Phone: 353 (0) 9 06 46 08 00

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KR3D0FRAK51X4SMTAHJAMPJP

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

Bladder catheter, Tiemann, 2 eyes14026704741899
Bladder catheter, Tiemann, 2 eyes14026704741912
Bladder catheter, Tiemann, 2 eyes14026704741882
Bladder catheter, Tiemann, 2 eyes14026704741929
Bladder catheter, Tiemann, 2 eyes14026704741936
Bladder catheter, Tiemann, 2 eyes14026704741875
Bladder catheter, Tiemann, 2 eyes14026704741905