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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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IQ Cath, Hydrophil, mit Urinbeutel — 14 UDI-DI variants, MDR

MD Atlas
Manfred Sauer GmbH

Data from EUDAMED, last updated May 23, 2026

IQ Cath, Hydrophil, mit Urinbeutel

42502745000012ED

14 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: Manfred Sauer GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42502745000012ED
Device name: IQ Cath, Hydrophil, mit Urinbeutel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: Manfred Sauer GmbH
SRN: DE-MF-000006287
Country: Germany
Email: info@manfred-sauer.de
Phone: +49 6226 960 100

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K8AS234AHDG2EA3G60C2Z93V

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

IQ2614.12-504250274540542
IQ2614.1204250274510460
IQ2614.1404250274510477
IQ2614.14-504250274540559
IQ2614.16-504250274540566
IQ2614.1604250274510484
IQ2604.1204250274510439
IQ2604.12-504250274540504
IQ2604.1404250274510446
IQ2604.14-504250274540511
IQ2604.1604250274510453
IQ2604.16-504250274540528
IQ2604.1804250274528106
IQ2604.18-504250274540535