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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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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

UDI-DI variants

36 UDI-DI variants

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Export results

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

MANUGIB trauma poignet T2G03322544747942
MANUGIB trauma poignet T3D03322544747928
MANUGIB trauma poignet T3G03322544747959
6527V-1D03322541900012
6527V-2D03322541900036
6527V-1G03322541900029
6527V-2G03322541900043
Orthèse de poignet T1D03322541022646
Orthèse de poignet T1G03322541022653
Orthèse de poignet T2D03322541022660
Orthèse de poignet T2G03322541022677

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