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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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Genuimmo 0° — 28 UDI-DI variants, MDR (THUASNE)

MD Atlas
THUASNE

Data from EUDAMED, last updated May 19, 2026

Genuimmo 0°

311179FR0140AER

28 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: THUASNE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 311179FR0140AER
Device name: Genuimmo 0°
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: THUASNE
SRN: FR-MF-000001201
Country: France
Email: service.conseil@thuasne.fr
Phone: +33 4 77 81 40 40

Variants by status

UDI-DI variants

28 UDI-DI variants

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Applied filters

basicUdiUlid01JXZWXZ9N5XP0J2TH0FMG9JNN

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

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2415025020500503111790109815
2425025030600503111790109914
2425012040600103111790239215
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2415025010500503111790109808
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2415025020600503111790109822
2425025040500503111790109921
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2425025020600503111790109891
2415025030500503111790109839
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2415012030600103111790239055
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2425012020600103111790239178
2415012030500103111790239048
2415025040600503111790109860
2415012010500103111790239017
2415025030600503111790109846
2415025040500503111790109853

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