86058

Organization name

DIESSE Diagnostica Senese S.p.A

SRN

IT-MF-000013311

Manufacturer status

Active

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

• CW008

  EUDAMED did not publish a description for this code.
• CW011

  EUDAMED did not publish a description for this code.
• CW265

  EUDAMED did not publish a description for this code.
• CW032

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.
• CW083

  EUDAMED did not publish a description for this code.

Primary placement in Italy; available across 1 country total.

Trade name

not provided

UDI-DI code

08033891323431

Basic UDI-DI

803389132CHORUSTTGA00FR

Reference / catalog number

86058

Issuing entity

GS1

Risk category

IVDR Class B

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

CHORUS tTg-A (REF. 86058 - 86058/12) is an immunoassay kit for automated semi-quantitative determination of IgA class antibodies against tissue Transglutaminase. Since anti-tTg antibodies show a high sensitivity and specificity for celiac disease, the kit is used as an aid to the related diagnosis and monitoring. The test, performed in human serum using a disposable device applied to the CHORUS/CHORUS TRIO/CHORUS EVO instruments, must be used by professional laboratory users only. It must be used by professional laboratory users only. The test is not intended to detect the exposure of the transmissible agent in blood, blood components, cells, tissues, organs or any derivative thereof for the purpose of assessing its suitability for transfusion, transplantation or cell administration.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

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

• W0102100601TISSUE TRANSGLUTAMINASE ANTIBODIES