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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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EASY SLIDE — 4 UDI-DI variants, IVDR (ARRAYTECH DIAGNOSTICS S.L.)

MD Atlas
ARRAYTECH DIAGNOSTICS S.L.

Data from EUDAMED, last updated May 23, 2026

EASY SLIDE

84370273150EASYSLIDEU9

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: ARRAYTECH DIAGNOSTICS S.L.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 84370273150EASYSLIDEU9
Device name: EASY SLIDE
Device model: EASY SLIDE
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Mar 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: ARRAYTECH DIAGNOSTICS S.L.
SRN: ES-MF-000042970
Country: Spain
Email: jzandbergen@arraytech.es
Phone: +34 918603594

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KK1BTJN1RK7A2TCE9B2TJVQJ

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

ES-1024-2508437027315053
ES-0124-2508437027315039
ES-0224-2508437027315107
ES-2024-108437027315091