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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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5 L DEMI-WATER — 2 UDI-DI variants, IVDR (YVSOLAB NV)

MD Atlas
YVSOLAB NV

Data from EUDAMED, last updated May 23, 2026

5 L DEMI-WATER

540700797SLWGD005YR

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: YVSOLAB NV

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 540700797SLWGD005YR
Device name: 5 L DEMI-WATER
Device model: 5 L DEMI-WATER
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Feb 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: YVSOLAB NV
SRN: BE-MF-000024599
Country: Belgium
Email: info@yvsolab.be
Phone: +32 14 67 27 79

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KGPHSFVPF564ETWMT6WP9T53

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

5 L EAU DEMINERALISEE / RECIPIENT EN PLASTIQUE05407007970308
5 L EAU DEMINERALISEE / RECIPIENT EN PLASTIQUE05407007970292