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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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MIMLED — 13 UDI-DI variants, MDR (MIMSAL TRADE, S.L.)

MD Atlas
MIMSAL TRADE, S.L.

Data from EUDAMED, last updated May 23, 2026

MIMLED

843656286MIMLEDQF

13 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: 843656286MIMLEDQF
Device name: MIMLED
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 24, 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

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KD5RX2338PKEQ97FF8P3Z9AP

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

ML1000C 100008436562861407
ML1000C 20008436562861469
ML1000C 40008436562861476
ML1000C 60008436562861483
ML1000C 80008436562861490
ML600C 100008436562861520
ML600C 20008436562861414
ML600C 40008436562861421
ML600C 60008436562861438
ML600C 80008436562861445
ML600FL08436562861056
ML600W08436562861049
ML1000W08436562861018