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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, Gel, mit Urinbeutel — 10 UDI-DI variants, MDR

MD Atlas
Manfred Sauer GmbH

Data from EUDAMED, last updated May 23, 2026

IQ Cath, Gel, mit Urinbeutel

42502745000014EH

10 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: 42502745000014EH
Device name: IQ Cath, Gel, mit Urinbeutel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 27, 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

10 UDI-DI variants

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Applied filters

basicUdiUlid01K8K147KM19D6E1CNJ51KJAK3

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

IQ3614.12-504250274541129
IQ3614.1204250274510644
IQ3614.14-504250274541136
IQ3614.1404250274510651
IQ3604.12-504250274541099
IQ3604.1204250274510613
IQ3604.1404250274510620
IQ3604.14-504250274541105
IQ3604.16-504250274541112
IQ3604.1604250274510637