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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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RIDASCREEN® Verotoxin — 5 UDI-DI variants, IVDR (R-Biopharm AG)

MD Atlas
R-Biopharm AG

Data from EUDAMED, last updated May 23, 2026

RIDASCREEN® Verotoxin

4049095C220100000HD

5 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: 4049095C220100000HD
Device name: RIDASCREEN® Verotoxin
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Sep 18, 2023

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

5 UDI-DI variants

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Applied filters

basicUdiUlid01HACAK5QMX7489S4XRD59T1XK

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

C2201K02-VK04049095030772
C220104049095030857
C2201K01-VK04049095030765
CRP220404049095030246
C2201C01-VK04049095030758