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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

1.0.0 — IVDR Class A IVDR by Engineering Ingegneria…

MD Atlas
Engineering Ingegneria Informatica S.p.A.

EUDAMED last updated this device on Mar 23, 2026

1.0.0

805516271ellipseLABBR

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Engineering Ingegneria Informatica S.p.A.
UDI-DI code: 08055162710047
Reference / catalog number: 1.0.0

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View device family (Basic UDI)

Manufacturer information

Organization name: Engineering Ingegneria Informatica S.p.A.
SRN: IT-MF-000038204
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08055162710047
Basic UDI-DI: 805516271ellipseLABBR
Reference / catalog number: 1.0.0
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: —
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

UDI-DI DataMatrix

Encoded

(01)08055162710047

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

W02079082VARIOUS GENERAL PURPOSE IVD INSTRUMENTS - SOFTWARE ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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Related devices

2.0.0805516271eRemoteCareBQOn the market

Certificates

Certificate health across this manufacturer's portfolio.

IT338973Supplemented
Quality management systemNotified body: 1370Expiry: Jan 9, 2030