Test d’antigène BinaxNOW™ Streptococcus pneumoniae

Le test d’antigène BinaxNOW™ S. pneumoniae est un test rapide destiné à la détection qualitative de l’antigène de S. pneumoniae dans l’urine de patients atteints de pneumonie et dans le liquide céphalo-rachidien (LCR) de patients atteints de méningite. Ce test est conçu pour faciliter le diagnostic de la pneumonie et de la méningite à pneumocoques, conjointement avec la mise en culture et les autres méthodes disponibles. Le test d’antigène urinaire BinaxNOW™ S. pneumoniae est visible directement sur la fenêtre de résultat ou peut être lu avec DIGIVAL™.

DIGIVAL™ avec carte antigène urinaire BinaxNOW™ Streptococcus pneumoniae est uniquement disponible sur certains marchés. Vente non autorisée aux États-Unis.

BinaxNOW Streptococcus pneumoniae Antigen Card BinaxNOW Streptococcus pneumoniae Antigen Card BinaxNOW Streptococcus pneumoniae Antigen Card

©2023 Abbott. All rights reserved. Unless otherwise specified, all product and service names appearing in this Internet site are trademarks owned by or licensed to Abbott, its subsidiaries or affiliates. No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company.

This website is governed by applicable U.S. laws and governmental regulations. The products and information contained herewith may not be accessible in all countries, and Abbott takes no responsibility for such information which may not comply with local country legal process, regulation, registration and usage.

Your use of this website and the information contained herein is subject to our Website Terms and Conditions and Privacy Policy. Photos displayed are for illustrative purposes only. Any person depicted in such photographs is a model. GDPR Statement | Declaration for California Compliance LawConditions Générales De Vente [pdf 175KB].

Not all products are available in all regions. Check with your local representative for availability in specific markets. For in vitro diagnostic use only. For i-STAT test cartridge information and intended use, refer to individual product pages or the cartridge information (CTI/IFU) in the i-STAT Support area.