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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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Incedo — 12 UDI-DI variants, MDR (Nordic-NeuroSTIM)

MD Atlas
Nordic-NeuroSTIM

Data from EUDAMED, last updated May 23, 2026

Incedo

5745000889_incedoYQ

12 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Nordic-NeuroSTIM

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5745000889_incedoYQ
Device name: Incedo
Device model: Incedo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Nordic-NeuroSTIM
SRN: DK-MF-000001363
Country: Denmark
Email: info@nordicneurostim.com
Phone: +45 31561520

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQYKHWK0H98FD5N68PGC34ER

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

Incedo05745000889006
Incedo Electrode Kit05745000889082
Incedo Foot Sensor Kit L05745000889112
Incedo Foot Sensor Kit M05745000889105
Incedo Foot Sensor Kit S05745000889099
Foot Sensor Kit XL05745000889129
Foot Sensor Trial Kit05745000889136
Treatment Kit L05745000889174
Treatment Kit M05745000889167
Treatment Kit XL05745000889181
Incedo Trial Kit B05745000889143
Treatment Kit S05745000889150