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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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ARNESES GORRO — 8 UDI-DI variants, MDR (MARTÍN VECINO, S.L.)

MD Atlas
MARTÍN VECINO, S.L.

Data from EUDAMED, last updated May 23, 2026

ARNESES GORRO

84354071ARNESGM2

8 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: MARTÍN VECINO, S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84354071ARNESGM2
Device name: ARNESES GORRO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: MARTÍN VECINO, S.L.
SRN: ES-MF-000013754
Country: Spain
Email: cristina.arranz@martinvecino-sl.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KCGR7GZTE8YDB6A48NY73MPE

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

M 07218435407103198
M 07318435407103211
M 08718435407106748
M 06218435407103174
M 16418435407107134
M 02118435407102344
M 01618435407102122
M 02818435407102467