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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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Wash buffer — 4 UDI-DI variants, IVDR (RefLab Aps)

MD Atlas
RefLab Aps

Data from EUDAMED, last updated May 31, 2026

Wash buffer

574400328WASHDP

4 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: RefLab Aps

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 574400328WASHDP
Device name: Wash buffer
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 24, 2022

Manufacturer & authorised representative

Manufacturer

Name: RefLab Aps
SRN: DK-MF-000021844
Country: Denmark
Email: info@reflab.dk
Phone: +45 7070 2345

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01G3BCE0ESXQF08NA4K1G26KFS

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

Wash buffer 200 mL05744003280155
Wash buffer 5 L05744003280162
Wash buffer concentrate 10 mL05744003280179
Wash buffer concentrate 50 mL05744003280186