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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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IndiTreat® ARRAYS — 3 UDI-DI variants, IVDR (2cureX A/S)

MD Atlas
2cureX A/S

Data from EUDAMED, last updated May 23, 2026

IndiTreat® ARRAYS

232118324ARRAYSZK

3 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: 2cureX A/S

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Device characteristics

ReagentProfessional testing

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 232118324ARRAYSZK
Device name: IndiTreat® ARRAYS
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Dec 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: 2cureX A/S
SRN: DK-MF-000036335
Country: Denmark
Email: support@2curex.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KCHBJDB1AXNH84EF8615AP6J

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

INDITREAT CRC EXPLORE ARRAY29418000012cxEXP
INDITREAT CRC EXTEND ARRAY29418000012cxEXT
INDITREAT CRC START ARRAY29418000012cxSTA