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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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Organization name
UDI-DI code
Reference / catalog number

ES-2024-1 — IVDR Class A IVDR by ARRAYTECH DIAGNOSTICS…

MD Atlas
ARRAYTECH DIAGNOSTICS S.L.

EUDAMED last updated this device on Mar 9, 2026

ES-2024-1

84370273150EASYSLIDEU9

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: ARRAYTECH DIAGNOSTICS S.L.
UDI-DI code: 08437027315091
Reference / catalog number: ES-2024-1

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Manufacturer information

Organization name: ARRAYTECH DIAGNOSTICS S.L.
SRN: ES-MF-000042970
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08437027315091
Basic UDI-DI: 84370273150EASYSLIDEU9
Reference / catalog number: ES-2024-1
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Liquid-based cytology processor for gynecological and non-gynecological specimens. Transfers cells from preservative solutions to slides using dual-membrane filter.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0580IVD GENERAL USE CONSUMABLES DEVICES - OTHER ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

ES-1024-2584370273150EASYSLIDEU9On the market ES-0124-2584370273150EASYSLIDEU9On the market ES-0224-2584370273150EASYSLIDEU9On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.