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Rapid fFN 10Q Diagnostic Device - Good Condition

Rapid fFN® 10Q is an in vitro diagnostic device for the quantitative detection of fetal fibronectin in cervicovaginal secretions. Used with the PeriLynx™ system or the Rapid fFN® 10Q system, it rapidly assesses the risk of preterm birth in pregnant women with signs of preterm labour. This test is essential for patients with intact amniotic membranes and minimal cervical dilation between 22 and 35 weeks of gestation. Rapid fFN® 10Q improves the management of preterm labour, thereby reducing the risk of preterm delivery.



Description

Rapid Assessment of Preterm Labour Risk with Rapid fFN® 10Q


Rapid fFN® 10Q is an in vitro diagnostic test designed for the quantitative detection of fetal fibronectin (fFN) in cervicovaginal secretions. This test is a crucial tool for rapidly assessing the risk of preterm birth in pregnant women with signs and symptoms of preterm labour. The test is particularly useful for patients with intact amniotic membranes and minimal cervical dilation (<3 cm), sampled between 22 weeks, 0 days and 35 weeks, 6 days of gestation.

Rapid fFN® 10Q is indicated for use as an aid in the rapid assessment of the risk of preterm birth in less than 34 weeks, 0 days of gestation in pregnant women with signs and symptoms of preterm labour, intact amniotic membranes, and minimal cervical dilation (<3 cm), sampled between 22 weeks, 0 days and 33 weeks, 0 days of gestation. In addition, it is indicated for assessing the risk of preterm birth at <30 weeks, <34 weeks, and <37 weeks of gestation in pregnant women at risk of preterm birth, sampled between 22 weeks, 0 days and 27 weeks, 6 days of gestation.

Women at risk of preterm labour include patients with a history of preterm labour or preterm rupture of membranes before 37 weeks, a history of spontaneous miscarriage in the second trimester, a history of cervical surgery such as LLETZ, LEEP, laser excision or conisation, and incidental discovery of a cervical length of 25 mm or less during the current pregnancy. These conditions may indicate an increased risk of complications during pregnancy, requiring careful monitoring and management.

The Rapid fFN® 10Q test represents a significant and necessary improvement in the ability to manage preterm labour that can lead to preterm birth. It offers a reliable and rapid solution for healthcare professionals, enabling better management of at-risk patients. By providing accurate quantitative results, this test enables doctors to make informed decisions about patient management, reducing the risk of preterm birth and improving outcomes for both mother and baby.

The Rapid fFN® 10Q is simple and effective to use, with a fast turnaround time , enabling rapid and appropriate intervention. This test is an essential tool in modern clinical practice, offering a reliable solution for assessing the risk of preterm labour and improving the management of at-risk patients. By incorporating this test into prenatal care protocols, healthcare professionals can provide better care for patients, thereby reducing complications associated with preterm labour.

Features

  • Rapid results: Provides results in less than 30 minutes
  • Ease of use: Simple to use with minimal training required
  • High accuracy: Offers high accuracy for reliable assessment of the risk of preterm birth
  • Compatibility: Compatible with the PeriLynx™ system and the Rapid fFN® 10Q system
  • Integrated quality control: Built-in quality controls to ensure reliable results

Technical Details

  • Storage temperature: 15°C to 30°C / 59°F to 86°F
  • Reaction time: 20 minutes
  • Sample volume: 200 μL

Compatible Accessories

  • Sample collection kit: Sample collection kit for foetal fibronectin
  • Positive and negative controls: Controls to ensure test performance
  • Pipettes: 200 μL pipettes for sample handling

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