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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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Aura Pretreat 3 — 2 UDI-DI variants, IVDR (ZytoVision GmbH)

MD Atlas
ZytoVision GmbH

Data from EUDAMED, last updated May 23, 2026

Aura Pretreat 3

4250380NHQE

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: ZytoVision GmbH

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 4250380NHQE
Device name: Aura Pretreat 3
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Mar 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: ZytoVision GmbH
SRN: DE-MF-000024390
Country: Germany
Email: info@zytovision.com
Phone: +49 (0)471 4832300

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KKTSWZECRYSBYM4QABS2BMPA

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

NOA-11504250380309965
NOA-10504250380309682