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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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Re5 Neuro Treatment System — 1 UDI-DI variant, MDR (Re5 ApS)

MD Atlas
Re5 ApS

Data from EUDAMED, last updated May 31, 2026

Re5 Neuro Treatment System

5745000441NTS02XD

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Re5 ApS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5745000441NTS02XD
Device name: Re5 Neuro Treatment System
Device model: Re5-NTS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 18, 2024

Manufacturer & authorised representative

Manufacturer

Name: Re5 ApS
SRN: DK-MF-000017805
Country: Denmark
Email: info@re5.com
Phone: +455053 1410

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01J0KHTEY3Y0D2BPT2DJKC1CYT

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

Re5 Neuro Treatment System05745000441099