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Cardiac D-Dimer Tests x10

ID:D6243 , 04877802190
GTIN:4015630052615

Roche Cardiac D-Dimer Test for DVT and PE Exclusion

The Roche Cardiac D-Dimer Test is a point-of-care test used in primary care, urgent care, and community clinical settings to support the exclusion of suspected deep vein thrombosis (DVT) or pulmonary embolism (PE). It is intended for use in parallel with a pre-test probability score and is designed for use with the Cobas h232 analyser. Each pack contains 10 tests.

Results are available within 8 minutes, with a measuring range of 0.1 to 4.0µg/mL and a cut-off value of 0.5µg/mL.

Product Features

  • 8-minute reaction time: results available within 8 minutes, supporting timely clinical decision-making at the point of care
  • Measuring range of 0.1–4.0µg/mL: defined quantitative range supports assessment across the clinically relevant D-Dimer spectrum
  • Cut-off value of 0.5µg/mL: standardised cut-off supports consistent application alongside pre-test probability scoring in DVT and PE exclusion pathways
  • For use with the Cobas h232 analyser: designated test for this device, supporting straightforward integration into existing point-of-care workflows
  • Pack of 10 tests: suited to lower-volume settings or as supplementary stock within existing DVT and PE assessment pathways

Product Specifications

  • Brand: Roche
  • Product Name: Cardiac D-Dimer Test
  • Compatible Analyser: Cobas h232
  • Pack Size: 10 tests
  • Reaction Time: 8 minutes
  • Measuring Range: 0.1–4.0µg/mL
  • Cut-Off Value: 0.5µg/mL
  • Intended Clinical Use: Point-of-care D-Dimer testing to support exclusion of suspected DVT or PE, used in parallel with pre-test probability score
  • Suitable Environments: GP practices, primary care clinics, urgent care settings, community clinical environments
  • Supplied By: Williams Medical Supplies

View our range of Diagnostic Supplies to support your point-of-care assessment pathways.

View the Product Information Notice advising you about CARDIAC D-Dimer assay and QC Compliance to IVD Regulation (EU) 2017/746

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