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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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ACCESSORIES — 9 UDI-DI variants, MDR (VOE , S.A)

MD Atlas
VOE , S.A

Data from EUDAMED, last updated May 23, 2026

ACCESSORIES

84353533ACCESSORIESLB

9 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: VOE , S.A

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84353533ACCESSORIESLB
Device name: ACCESSORIES
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: VOE , S.A
SRN: ES-MF-000013290
Country: Spain
Email: info@voe.es
Phone: 934516452

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01JS1VKDZZZS7P4PT1SCS9ERHJ

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

6100 L08435353340145
6100 M08435353340138
6100 S08435353340121
6100 T08435353340114
6101 L08435353340237
6101 M08435353340220
6101 S08435353340213
6101 T08435353340206
8000 T/U08435353339866