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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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LUXIFLEX II — 4 UDI-DI variants, MDR (MIMSAL TRADE, S.L.)

MD Atlas
MIMSAL TRADE, S.L.

Data from EUDAMED, last updated May 23, 2026

LUXIFLEX II

843656286LUXIIRJ

4 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: MIMSAL TRADE, S.L.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 843656286LUXIIRJ
Device name: LUXIFLEX II
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: MIMSAL TRADE, S.L.
SRN: ES-MF-000039030
Country: Spain
Email: regulatory@mimsal.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JV5RX099YCN2398GP408GBKX

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

LX237008436562860608
LX2370P08436562860615
LX2324S08436562860622
LX2324SP08436562860639