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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

Easy-NAT — IVDR Class A IVDR by Eurospital Spa

MD Atlas
Eurospital Spa

EUDAMED last updated this device on Apr 22, 2026

Easy-NAT

802816920AW02060609015C

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Eurospital Spa
UDI-DI code: 08028169207711
Reference / catalog number: 9151

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View device family (Basic UDI)

Manufacturer information

Organization name: Eurospital Spa
SRN: IT-MF-000028468
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	May 18, 2022	Still on market

Device identification

Trade name: Easy-NAT
UDI-DI code: 08028169207711
Basic UDI-DI: 802816920AW02060609015C
Reference / catalog number: 9151
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: Easy-NAT is an IVD middleware for the management of diagnostic tools and data in the physiological and pathological field. Intended for laboratories engaged in molecular diagnostics for professional use only.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

W02069082VARIOUS SAMPLE PROCESSING INSTRUMENTS - SOFTWARE ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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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.