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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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RIDA®QUICK IFX Monitoring — 2 UDI-DI variants, IVDR (R-Biopharm AG)

MD Atlas
R-Biopharm AG

Data from EUDAMED, last updated May 23, 2026

RIDA®QUICK IFX Monitoring

4049095GN30410000AN

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class C

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Manufacturer: R-Biopharm AG

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 4049095GN30410000AN
Device name: RIDA®QUICK IFX Monitoring
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Jun 26, 2024

Manufacturer & authorised representative

Manufacturer

Name: R-Biopharm AG
SRN: DE-MF-000007993
Country: Germany
Email: t.zeugfang@r-biopharm.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01J1AD2KWHB48PMG39AFS53PHJ

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

GP304104049095070174
GN304104049095070167