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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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VisualSystem HD — 4 UDI-DI variants, MDR (NordicNeuroLab AS)

MD Atlas
NordicNeuroLab AS

Data from EUDAMED, last updated May 31, 2026

VisualSystem HD

7090042052016Z

4 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: NordicNeuroLab AS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 7090042052016Z
Device name: VisualSystem HD
Device model: VSHD 1.3
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: NordicNeuroLab AS
SRN: NO-MF-000000555
Country: Norway
Email: chandana@nordicneurolab.com
Phone: 4741766239

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JNKCS8VN2XEKJRRQM1BNGZJC

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

Control Room Interface (CRI)07090042052061
Visual System Power Supply (VPS)07090042052122
VisualSystem HD07090042052115
VisualSystem Power Cable (VPC)07090042052078