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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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Detect 2 — 3 UDI-DI variants, MDR (OneLife SA)

MD Atlas
OneLife SA

Data from EUDAMED, last updated May 31, 2026

Detect 2

54250394OL23K7

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: OneLife SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 54250394OL23K7
Device name: Detect 2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: OneLife SA
SRN: BE-MF-000003821
Country: Belgium
Email: info@onelife-bf.com
Phone: 0475332147

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KRSCWFEQA6T8V9C02FEBN9PM

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

Detect 2 colorant 2x5L05425039491127
Detect 2 colorant 6x950ml05425039491141
Detect 2 kit05425039491134