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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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CITOSCANN® — 8 UDI-DI variants, IVDR (QUIMICA CLINICA APLICADA S.A.)

MD Atlas
QUIMICA CLINICA APLICADA S.A.

Data from EUDAMED, last updated May 23, 2026

CITOSCANN®

8430155CITOSCANNFV

8 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: QUIMICA CLINICA APLICADA S.A.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 8430155CITOSCANNFV
Device name: CITOSCANN®
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: QUIMICA CLINICA APLICADA S.A.
SRN: ES-MF-000001512
Country: Spain
Email: rtec@qca.es
Phone: +34977701439

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HM92Q7B1DS9E0TPW7W4HAKZJ

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

990300 08430155005773
999701 08430155006220
99415008430155005933
99415608430155010197
99414008430155005926
994190 08430155005940
999525 08430155006213
99771108430155006114