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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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BENFIX TRIPLE ACCION 50 g — 6 UDI-DI variants, MDR

MD Atlas
Laboratorios URGO S.L.

Data from EUDAMED, last updated May 23, 2026

BENFIX TRIPLE ACCION 50 g

8413647ULTRASINSABORVZ

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: Laboratorios URGO S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8413647ULTRASINSABORVZ
Device name: BENFIX TRIPLE ACCION 50 g
Device model: FÓRMULA ULTRAFUERTE SIN SABOR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 26, 2022

Manufacturer & authorised representative

Manufacturer

Name: Laboratorios URGO S.L.
SRN: ES-MF-000000629
Country: Spain
Email: administracion@es.urgo.com
Phone: +34 943 33 50 57

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01GG9Y6XFG14ZS5FWHBEMXPR08

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

ES000374208413647037421
ES000367008413647036707
Livsane08413647038794
ES000525808413647052585
ES000525908413647052592
ES000528908413647052899