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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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Genou dv4 beige GIBORTHO T1 — 10 UDI-DI variants, MDR (GIBAUD)

MD Atlas
GIBAUD

Data from EUDAMED, last updated May 19, 2026

Genou dv4 beige GIBORTHO T1

332254043KQ

10 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: 332254043KQ
Device name: Genou dv4 beige GIBORTHO 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

10 UDI-DI variants

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Applied filters

basicUdiUlid01KEV7933AXK87M35BHKMYMQYY

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

Genou dv4 anthracite GIBORTHO T103322541023698
Genou dv4 anthracite GIBORTHO T203322541023704
Genou dv4 anthracite GIBORTHO T303322541023711
Genou dv4 anthracite GIBORTHO T403322541023728
Genou dv4 anthracite GIBORTHO T503322541023735
Genou dv4 beige GIBORTHO T103322541023643
Genou dv4 beige GIBORTHO T203322541023650
Genou dv4 beige GIBORTHO T303322541023667
Genou dv4 beige GIBORTHO T403322541023674
Genou dv4 beige GIBORTHO T503322541023681