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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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viQtor System — 4 UDI-DI variants, MDR (smartQare BV)

MD Atlas
smartQare BV

Data from EUDAMED, last updated May 30, 2026

viQtor System

87202995724vQsystem01SG

4 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: smartQare BV

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 87202995724vQsystem01SG
Device name: viQtor System
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 6, 2025

Manufacturer & authorised representative

Manufacturer

Name: smartQare BV
SRN: NL-MF-000003491
Country: Netherlands
Email: reinier.vrolijk@smartqare.nl
Phone: +31 651447496

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K6W6ZRP24PFMWVN0SFGMBCH0

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

viQtor08720299572409
viQtor App 08720299572430
viQtor Platform08720299572423
viQtor System08720299572461