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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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VIDAL Sécurisation — 180 UDI-DI variants, MDR (VIDAL FRANCE)

MD Atlas
VIDAL FRANCE

Data from EUDAMED, last updated May 19, 2026

VIDAL Sécurisation

3666075VSECU000001FS

180 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: VIDAL FRANCE

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3666075VSECU000001FS
Device name: VIDAL Sécurisation
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Feb 20, 2024

Manufacturer & authorised representative

Manufacturer

Name: VIDAL FRANCE
SRN: FR-MF-000004612
Country: France
Email: service.clients@vidal.fr

Variants by status

UDI-DI variants

180 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HQ3C0XA2FCQKSVSRMD5E2NXR

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

2025.12.503666075007282
2025.11.103666075006117
VIDAL Sécurisation03666075000962
VIDAL Sécurisation03666075000320
VIDAL Sécurisation03666075000696

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