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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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ACTI'TAB — 6 UDI-DI variants, MDR (BENOIT SYSTEMES)

MD Atlas
BENOIT SYSTEMES

Data from EUDAMED, last updated May 19, 2026

ACTI'TAB

376034429ACTITABFN

6 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: BENOIT SYSTEMES

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376034429ACTITABFN
Device name: ACTI'TAB
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: BENOIT SYSTEMES
SRN: FR-MF-000004445
Country: France
Email: contact@benoitsystemes.com
Phone: 03 80 96 51 25

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01K4ADRTG56JTBNY57584DEASN

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

Acti'tab enfant droit03760344290075
Acti'tab enfant gauche03760344290068
Acti'tab large droit03760344290051
Acti'tab large gauche03760344290044
Acti'tab standard droit03760344290099
Acti'tab standard gauche03760344290082