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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 — 90 UDI-DI variants, MDR (Manfred Sauer GmbH)

MD Atlas
Manfred Sauer GmbH

Data from EUDAMED, last updated May 23, 2026

IQ Cath, Hydrophil

42502745000011EB

90 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: 42502745000011EB
Device name: IQ Cath, Hydrophil
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 31, 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

90 UDI-DI variants

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Applied filters

basicUdiUlid01K8WYQWHCM36F39FAFGPVVV3N

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

IQ2304.1204250274543574
IQ2304.12-504250274544021
IQ2304.1404250274543581
IQ2304.14-504250274544038
IQ2304.1604250274543598
IQ2304.16-504250274544045
IQ2304.18-504250274544052
IQ4304.1004250274518978
IQ4304.10-504250274544113
IQ4304.12-504250274544120
Q4304.1204250274518992
IQ4304.16-504250274544144
IQ4304.1604250274519111
IQ4304.18-504250274544151
IQ4304.1804250274542607

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