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Associé à un tube d’analyse cobas® Liat® , l’instrument effectue la préparation des réactifs, l’enrichissement des cibles, l’élimination des inhibiteurs, l’extraction des acides nucléiques, l’amplification par PCR, la détection en temps réel et l’interprétation de résultats afin d’automatiser la détection ou la quantification des cibles d’acides nucléiques dans un échantillon biologique.
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Système cobas® Liat®

Système cobas® Liat®
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Nous mettons tout un laboratoire dans un tube.

Petit : l'analyseur, plus petit qu'une boîte à chaussures (Hauteur 19.0 cm, Largeur 11.4 cm, Longueur 24.1 cm) convient particulièrement lorsque l’espace est limité.

 

Simplicité : le système cobas® Liat® est entièrement automatisé. Il est piloté par le biais d’un écran tactile et ne nécessite qu’une formation minimale des utilisateurs et un faible temps de manipulation. 

 

Sûr : La conception permet le scellement des tubes, éliminant ainsi le contact entre l’utilisateur et les réactifs et autres produits chimiques. Le système d’analyse entièrement fermé et les nombreux systèmes de contrôle et de surveillance réduisent le potentiel d’erreurs de manipulation.

 

Connecté : Le système  cobas® Liat® offre une connectivité bidirectionnelle permettant d'utiliser le système en laboratoire comme en délocalisé tout en étant connecté.

Fonctionnalité du système de PCR cobas® Liat®

Le système cobas® Liat® détecte l’ADN (ou l’ARN) d’un agent infectieux recherché à partir des échantillons de patients. Le portefeuille de tests comprend cobas® Cdiff, cobas® Strep A, cobas® Influenza A/B et cobas® Influenza A/B & RSV. Le système d’analyse est entièrement fermé, réduisant ainsi le risque de contamination, pour une sécurité sans faille. Protégée par un ensemble de dispositifs de contrôles, cette innovation garantit des tests de PCR de qualité. Les tests à base d'acides nucléiques sont entièrement automatisés.

Performance du système de PCR cobas® Liat®

Le système  cobas® Liat® permet l’obtention des résultats en 20 minutes. Grâce à la technologie PCR de Roche, le niveau de sensibilité et de spécificité des tests est similaire à celui obtenu dans un laboratoire ce qui réduit considérablement le risque de faux négatifs et de faux positifs. Pas besoin d'interprétation ni de confirmation.

Simplification des processus de PCR grâce au système cobas® Liat®

 

Le système cobas® Liat®est composé d'un tube de test et de l'analyseur cobas® Liat®, et fournit des résultats aussi précis que ceux obtenus en laboratoire en seulement 15 à 20 minutes en fonction du paramètre testé. Le temps de manipulation est inférieur à une minute.

Le test STAT cobas® Liat® PCR analyse l'échantillon du patient.
La simplification des flux de travail PCR fait partie des avantages du système cobas® Liat®.
Ce test appartient à la gamme de tests PCR automatisés.

Échantillon

 

La pipette de transfert fournie permet de transférer l'échantillon du patient dans le tube à essai.

Scanner

 

L’analyseur cobas® Liat® possède un lecteur de code-barres intégré permettant l'identification de l'échantillon du patient.

Rapidité

 

Les résultats sont produits rapidement:

  • 15 min : Strep A1
  • 20 min : Influenza A/B2, Influenza A/B & RSV et SARS-COv23
Contactez votre représentant local pour en savoir plus
CONTACTEZ-NOUS

Références :

  1. Notice cobas® Strep A v4 02/2020
  2. Notice cobas® Influenza A/B & RSV v5 10/2020
  3. Notice cobas® Influenza A/B & SARS CoV2 v2 10/2020

Le cobas® Liat® Analyzer est un instrument automatisé de test des acides nucléiques qui, lorsqu’il est utilisé conjointement avec les tubes d’analyse cobas® Liat® pour effectuer des tests de diagnostic in vitro, est désigné par l’appellation cobas® Liat®  System. Associé à un tube d’analyse cobas® Liat®, l’instrument effectue la préparation des réactifs, l’enrichissement des cibles, l’élimination des inhibiteurs, l’extraction des acides nucléiques, l’amplification par PCR, la détection en temps réel et l’interprétation de résultats afin d’automatiser la détection ou la quantification des cibles d’acides  nucléiques dans un échantillon biologique.
Dispositif médical de diagnostic in vitro. Classe A
Mandataire : Roche Diagnostics GmbH (Allemagne) – Distributeur : Roche Diagnostics France
Lire attentivement les instructions figurant dans le manuel d’utilisation.

Mis à jour : 09/2022

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