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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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SECURIDRAP® SELFIA® — 8 UDI-DI variants, MDR (Groupe Mulliez-Flory)

MD Atlas
Groupe Mulliez-Flory

Data from EUDAMED, last updated May 19, 2026

SECURIDRAP® SELFIA®

361105SECURIDRAPY8

8 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: Groupe Mulliez-Flory

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 361105SECURIDRAPY8
Device name: SECURIDRAP® SELFIA®
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 1, 2022

Manufacturer & authorised representative

Manufacturer

Name: Groupe Mulliez-Flory
SRN: FR-MF-000009487
Country: France
Email: contact@mulliez-flory.fr
Phone: 0241637810

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01GBQGBG2ADG563N7DNDGGNJWZ

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

SÉCURIDRAP® SELFIA®03611057575273
SÉCURIDRAP® SELFIA®03611057575464
SÉCURIDRAP® SELFIA®03611057575303
SÉCURIDRAP® SELFIA®03611057575457
SÉCURIDRAP® SELFIA®03611057575280
SÉCURIDRAP® SELFIA®03611057575297
SÉCURIDRAP® SELFIA®03611057575471
SÉCURIDRAP® SELFIA®03611057575488