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Organization name
UDI-DI code
Reference / catalog number

DSC 5522-DCP — Class I MDR by EIZO GmbH

MD Atlas
EIZO GmbH

EUDAMED last updated this device on Mar 10, 2025

DSC 5522-DCP

42513033MonitorIVRadKG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EIZO GmbH
UDI-DI code: 04251303302186
Reference / catalog number: DSC 5522-DCP

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Manufacturer information

Organization name: EIZO GmbH
SRN: DE-MF-000014106
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW273
Caution: Risk of electric shock. Do not open.
CW999
The monitor is not suitable for mammography.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Feb 27, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04251303302186
Basic UDI-DI: 42513033MonitorIVRadKG
Reference / catalog number: DSC 5522-DCP
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Intended Purpose: The product is intended for the display of still images and moving images from various commercially available devices commonly used in a medical environment, in particular radiology. The monitor is optimized for the reproduction of grayscale X-ray images. The monitor is not suitable for mammography. Technical datas: 55 (139cm) color Monitor 3840 x 2160 native resolution Panel technology :IPS LCD panel High bright Video input: DVI, DisplayPort 1.1 and 1.2 On Screen Display for setup and control VESA 400x400 mount Brightness stability controlled DICOM calibrated integrated Protection screen
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z11900802BIOIMAGING VIEWING MONITORS

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.

Related devices

This device is not currently linked to any other device.