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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

ImgView — Class IIa MDR by RAR s.r.l.

MD Atlas
RAR s.r.l.

EUDAMED last updated this device on Apr 29, 2026

ImgView

805759209IMGVIEWXU

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: RAR s.r.l.
UDI-DI code: 08057592090010
Reference / catalog number: ImgView

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View device family (Basic UDI)

Manufacturer information

Organization name: RAR s.r.l.
SRN: IT-MF-000030103
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.

Country	On market since	Until
ItalyPrimary placement	Jul 14, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08057592090010
Basic UDI-DI: 805759209IMGVIEWXU
Reference / catalog number: ImgView
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on 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)08057592090010

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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.

Z11030692COMPUTED TOMOGRAPHS (CT) - MEDICAL DEVICE SOFTWARE

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Related devices

ARTiCAT805759209AC01BZOn the market

Certificates

Certificate health across this manufacturer's portfolio.

ITH 2453837 1Supplemented
Quality management systemNotified body: 1936Expiry: Jul 20, 2028