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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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QVINTETT Vårdsäng CS4 — 7 UDI-DI variants, MDR

MD Atlas
ComfortSystem Scandinavia AB

Data from EUDAMED, last updated May 30, 2026

QVINTETT Vårdsäng CS4

735000589QHCS48U

7 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: ComfortSystem Scandinavia AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 735000589QHCS48U
Device name: QVINTETT Vårdsäng CS4
Device model: QVINTETT Vårdsäng CS4
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: ComfortSystem Scandinavia AB
SRN: SE-MF-000038482
Country: Sweden
Email: andreas.rickman@comfortsystem.se
Phone: +463651590

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS7M2DEPW6D99Q9N0Y56QJ3B

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

HL100F-207350005890100
QH105H100Q07350005890063
QH120H100Q07350005890070
QH090H100Q-Lyft07350005897246
QH090H100Q07350005897253
QH120HL100F-207350005890094
QH105HL100F-207350005890087