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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 Blood DNA Kit – PP Mini (MDX) — 4 UDI-DI variants, IVDR

MD Atlas
IST Innuscreen GmbH

Data from EUDAMED, last updated May 23, 2026

deltaPREP Blood DNA Kit – PP Mini (MDX)

4262375220058R

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: 4262375220058R
Device name: deltaPREP Blood DNA Kit – PP Mini (MDX)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Oct 28, 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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Export results

Applied filters

basicUdiUlid01K8MT6XXZ9M7TWDTNYE9FHMJD

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 Blood DNA Kit – PP Mini (MDX) Strip 16 rxn04262375225051
- deltaPREP Blood DNA Kit – PP Mini (MDX) Strip 96 rxn04262375225068
deltaPREP Blood DNA Kit – PP Mini (MDX)04262375225013
deltaPREP Blood DNA Kit – PP Mini (MDX) Plate 96 rxn04262375225020