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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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Miamind Neurostimulator Electrodes — 2 UDI-DI variants, MDR

MD Atlas
Bottneuro AG

Data from EUDAMED, last updated May 23, 2026

Miamind Neurostimulator Electrodes

76499880355ELECTNF

2 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: Bottneuro AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 76499880355ELECTNF
Device name: Miamind Neurostimulator Electrodes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 30, 2024

Manufacturer & authorised representative

Manufacturer

Name: Bottneuro AG
SRN: CH-MF-000041419
Country: Switzerland
Email: mail@bottneuro.ch
Phone: +41 61 515 00 43

Authorised representative

Name: Blue Broccoli GmbH
SRN: LI-AR-000000233
Country: Liechtenstein

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HWQJM4R8P0B7G7WAFJD962WA

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

Electrode Gel Adapter07649988035524
Miamind Neurostimulator Electrode07649988035517