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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 3D D T1D — 36 UDI-DI variants, MDR (GIBAUD)

MD Atlas
GIBAUD

Data from EUDAMED, last updated May 19, 2026

MANUGIB 3D D T1D

332254035KR

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: 332254035KR
Device name: MANUGIB 3D D T1D
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

basicUdiUlid01KEV71A4E342J9E8D3AGSJ96Z

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

6701V-2G03322541069269
6701V-3G03322541069276
6701V-4G03322541069283
6701V-5G03322541069290
6701V-6G03322541069306
6701VB-1G03322541080264
6701VB-2G03322541080271
6701VB-3G03322541080288
6701VB-4G03322541080295
6701VB-5G03322541080301
6701VB-6G03322541080318

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