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

MD Atlas
MIMSAL TRADE, S.L.

Data from EUDAMED, last updated May 23, 2026

VISTA

843656286VISTAS4

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: 843656286VISTAS4
Device name: VISTA
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

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KDMP2Z8Q3YVNV6HXZ2S3ACH5

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

E0051L08436562860462
E051PL08436562860479
E051CAO01208436562860028
E051LAT21208436562860035