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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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LUPA — 7 UDI-DI variants, MDR (MIMSAL TRADE, S.L.)

MD Atlas
MIMSAL TRADE, S.L.

Data from EUDAMED, last updated May 23, 2026

LUPA

843656286LUPAPA

7 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843656286LUPAPA
Device name: LUPA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 29, 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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KDMKEY8BJ2YRY9XWXE5A97HV

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

09332-308436562860561
09332-808436562860578
0933208436562860066
09340C08436562860646
0934008436562860073
09340-308436562860509
09340-808436562860516