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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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INSTANT Virus RNA/DNA Kit — 2 UDI-DI variants, IVDR (Roboscreen GmbH)

MD Atlas
Roboscreen GmbH

Data from EUDAMED, last updated May 23, 2026

INSTANT Virus RNA/DNA Kit

426238673025920HW

2 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Roboscreen GmbH

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 426238673025920HW
Device name: INSTANT Virus RNA/DNA Kit
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Roboscreen GmbH
SRN: DE-MF-000024661
Country: Germany
Email: info@roboscreen.com
Phone: +49(0)3419897340

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KRXPRA0NGBAGH9FSZ03QHRWE

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

847-025920060304262386730018
847-025920060204262386730001