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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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Dispositif de liposuccion non stérile… — 2 UDI-DI variants, MDR

MD Atlas
EUROMI

Data from EUDAMED, last updated May 23, 2026

Dispositif de liposuccion non stérile / Non sterile liposuction equipment

3701416260000EVA5J

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: EUROMI

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Device characteristics

Active deviceReusable

Identity & classification

Basic UDI-DI: 3701416260000EVA5J
Device name: Dispositif de liposuccion non stérile / Non sterile liposuction equipment
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: EUROMI
SRN: BE-MF-000014212
Country: Belgium
Email: info@euromi.com
Phone: +32 87 29 22 22

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS2ERMJ5V7N056DPKP3JEED3

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

1127ADIPC03701416203425
1127ADIPC11003701416203432