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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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GenuExtrem — 6 UDI-DI variants, MDR (THUASNE)

MD Atlas
THUASNE

Data from EUDAMED, last updated May 19, 2026

GenuExtrem

311179FR0120AEF

6 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: 311179FR0120AEF
Device name: GenuExtrem
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

6 UDI-DI variants

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Applied filters

basicUdiUlid01JXZX0CTP1QGG8CPMXQAC9JEB

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

2321022030019903111797400656
2321022050019903111797400670
2321022010019903111797400632
2321022020019903111797400649
2321022060019903111797400687
2321022040019903111797400663