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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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GENUGIB ARTHROSE T1 — 6 UDI-DI variants, MDR (GIBAUD)

MD Atlas
GIBAUD

Data from EUDAMED, last updated May 19, 2026

GENUGIB ARTHROSE T1

332254042KN

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: GIBAUD

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 332254042KN
Device name: GENUGIB ARTHROSE T1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: GIBAUD
SRN: FR-MF-000014279
Country: France
Email: frederique.guentleur@innothera.com
Phone: +33146152957

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KEV728JSZ4F5D7KBP65PN37X

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

GENUGIB ARTHROSE T103322541070463
GENUGIB ARTHROSE T203322541070470
GENUGIB ARTHROSE T303322541070487
GENUGIB ARTHROSE T403322541070494
GENUGIB ARTHROSE T503322541070500
GENUGIB ARTHROSE T603322541070517