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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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JUST UNIC® — 9 UDI-DI variants, MDR (EVOLUTIS)

MD Atlas
EVOLUTIS

Data from EUDAMED, last updated May 19, 2026

JUST UNIC®

376025538L091101rV5

9 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: EVOLUTIS

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 376025538L091101rV5
Device name: JUST UNIC®
Device model: JUST UNIC®
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 12, 2024

Manufacturer & authorised representative

Manufacturer

Name: EVOLUTIS
SRN: FR-MF-000000492
Country: France
Email: qualite@evolutis-group.com

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HKY9J42AAJS4SCEAKB5DAXPZ

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

JUST UNIC®03701271025347
JUST UNIC®03701271024951
JUST UNIC®03701271025378
JUST UNIC®03701271025385
JUST UNIC®03701271027020
JUST UNIC®03701271025354
JUST UNIC®03701271025361
JUST UNIC®03701271024968
JUST UNIC®03701271024944