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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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Electrodes — 3 UDI-DI variants, MDR (Neuroelectrics Barcelona, S.L.U.)

MD Atlas
Neuroelectrics Barcelona, S.L.U.

Data from EUDAMED, last updated May 23, 2026

Electrodes

8436612820MF06Electrode9Y

3 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: Neuroelectrics Barcelona, S.L.U.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8436612820MF06Electrode9Y
Device name: Electrodes
Device model: Electrodes - EEG + tES
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 3, 2024

Manufacturer & authorised representative

Manufacturer

Name: Neuroelectrics Barcelona, S.L.U.
SRN: ES-MF-000033432
Country: Spain
Email: info@neuroelectrics.com
Phone: +34 932540366

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01J1WN3J2X8QNVKBV95QX0QDJQ

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

NE027-P.01.MD:GV18437017440434
NE029-P.01.MD:GV18437017440403
NE029-P.08.MD:GV18437017440496