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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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MANUGIB trauma poignet T0D — 36 UDI-DI variants, MDR (GIBAUD)

MD Atlas
GIBAUD

Data from EUDAMED, last updated May 19, 2026

MANUGIB trauma poignet T0D

332254029KW

36 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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UDI-DI variants

36 UDI-DI variants

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Applied filters

basicUdiUlid01KEV71AAXQSWSC8AXXMA0E479

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

6508VX-0D03322541071286
6508VX-1D03322541071293
6508VX-2D03322541071309
6508VX-3D03322541071316
6508VX-0G03322541071323
6508VX-1G03322541071330
6508VX-2G03322541071347
6508VX-3G03322541071354
MANUGIB Tendinite T1D03322541040121
MANUGIB Tendinite T1G03322541040138
MANUGIB Tendinite T2D03322541040145
MANUGIB Tendinite T2G03322541040152
MANUGIB Tendinite T3D03322541040169
MANUGIB Tendinite T3G03322541040176
MANUGIB Trauma poignet long T0D03322541028976
MANUGIB Trauma poignet long T0G03322541028983
MANUGIB Trauma poignet long T1D03322541028990
MANUGIB Trauma poignet long T1G03322541029003
MANUGIB Trauma poignet long T2D03322541029010
MANUGIB Trauma poignet long T2G03322541029027
MANUGIB trauma poignet T0D03322541015747
MANUGIB trauma poignet T0G03322541015754
MANUGIB trauma poignet T1D03322544747904
MANUGIB trauma poignet T1G03322544747935
MANUGIB trauma poignet T2D03322544747911

1 2

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 332254029KW
Device name: MANUGIB trauma poignet T0D
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