TarCET Kit Aortopathy Panel

Organization name

MEDICOVER GENETICS LIMITED

SRN

CY-MF-000009381

Manufacturer status

Active

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

• CW082

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• CW401

  In all cases of doubt, or when symptoms persist, seek medical advice. Immediate medical attention is not required.
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• CW999

  P501 - Dispose of contents/container to hazardous or special waste collection point, in accordance with local, regional, national and/or international regulation.
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Primary placement in Cyprus; available across 1 country total.

Trade name

TarCET Kit Aortopathy Panel

UDI-DI code

05298004820228

Basic UDI-DI

52980048MULTITN

Reference / catalog number

ET203-00-2016

Issuing entity

GS1

Risk category

IVDR Class A

Applicable legislation

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]

Status

On the market

Quantity

1

Additional product description

Refer to IFU [EN]

Additional information URL

https://medicover-genetics.com/partner-with-us/tarcet-kits/tarcet-kit-panels/

Clinical sizes

No clinical sizes registered for this device.

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

• W01060299TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER