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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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deltaPREP Virus PLUS Kit -… — 4 UDI-DI variants, IVDR

MD Atlas
IST Innuscreen GmbH

Data from EUDAMED, last updated May 23, 2026

deltaPREP Virus PLUS Kit - Multi-Device 96 (MDX)

4262375220048P

4 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: IST Innuscreen GmbH

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 4262375220048P
Device name: deltaPREP Virus PLUS Kit - Multi-Device 96 (MDX)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Mar 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: IST Innuscreen GmbH
SRN: DE-MF-000024606
Country: Germany
Email: info.innu@ist-ag.com
Phone: +494903094893380

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01HV65GE3Z52SHMAZH9R1XYHKT

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

deltaPREP Virus PLUS Kit - Multi-Device 96 (MDX) (480 rxn)04262375224023
deltaPREP Virus PLUS Kit - Multi-Device 96 (MDX) (96 rxn)04262375224016
PurePrep Path DX Kit (480 rxn)04262375224054
PurePrep Path DX Kit (96 rxn)04262375224047