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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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ZytoLight SPEC CDKN2A/CEN 3/7/17… — 2 UDI-DI variants, IVDR

MD Atlas
ZytoVision GmbH

Data from EUDAMED, last updated May 23, 2026

ZytoLight SPEC CDKN2A/CEN 3/7/17 Quadruple Color Probe

4250380P125QS

2 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: ZytoVision GmbH

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Device characteristics

ReagentProfessional testingHuman tissues / cellsAnimal tissues / cells

Identity & classification

Basic UDI-DI: 4250380P125QS
Device name: —
Device model: ZytoLight SPEC CDKN2A/CEN 3/7/17 Quadruple Color Probe
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Apr 30, 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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Applied filters

basicUdiUlid01KQEDKS0W2ZES2ZF7688Z0B75

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

Z-2081-5004250380302119
Z-2081-20004250380302201