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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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Quicklysis™ — 2 UDI-DI variants, IVDR (CYTOGNOS, S.L)

MD Atlas
CYTOGNOS, S.L

Data from EUDAMED, last updated May 23, 2026

Quicklysis™

8436548980089C9

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: CYTOGNOS, S.L

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 8436548980089C9
Device name: Quicklysis™
Device model: Quicklysis™
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 30, 2022

Manufacturer & authorised representative

Manufacturer

Name: CYTOGNOS, S.L
SRN: ES-MF-000000318
Country: Spain
Email: direction@cytognos.com
Phone: +34 923125067

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G4AVC9RRN0TR3Q892Z465Z87

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

CYT-QL-108436548981075
CYT-QL-308436548981099