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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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CubePlus — 3 UDI-DI variants, IVDR (opTricon GmbH)

MD Atlas
opTricon GmbH

Data from EUDAMED, last updated May 23, 2026

CubePlus

42520204CPLUSAP

3 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: opTricon GmbH

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Device characteristics

Near-patient testingProfessional testing

Identity & classification

Basic UDI-DI: 42520204CPLUSAP
Device name: CubePlus
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Nov 11, 2024

Manufacturer & authorised representative

Manufacturer

Name: opTricon GmbH
SRN: DE-MF-000024656
Country: Germany
Email: info@optricon.de

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JCDD4SH5RXG8XQVN42Y70ZTX

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

CubePlus04252020400131
CubePlus04252020400162
CubePlus04252020400155