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LIMITED WARRANTY
This warranty gives you specific legal rights. Additionally, you may have other rights that vary from region to region.
The BD Veritor™ Plus Analyzer, BD Veritor™ InfoScan Module, BD Veritor™ Plus Connect, and BD Veritor™ InfoWiFi module are warranted
to be free from defects in materials and workmanship for a period of two years following delivery. BD’s sole responsibility under this warranty
shall be to repair or replace any instrument or its components (except for expendable supplies) which under normal operating conditions,
prove to be defective within two years of delivery.
BD will furnish new or re-manufactured components upon its option. All replacements shall meet new part specifications. Replaced
components become the property of BD.
It is understood that the equipment covered by this warranty has been installed in accordance with the recommendations and instructions in
the BD Veritor™ Plus Analyzer Instructions for Use Manual.
Any damage to a BD Veritor™ Plus Analyzer resulting from the failure of the owner to maintain reasonable care and precautions in the
operation and maintenance of the system will void this warranty and terminate the obligations of the manufacturer as stated herein.
This warranty is in lieu of all other warranties, whether express or implied, including but not limited to, warranties of merchantability, or fitness
for a particular use. In no event will BD Diagnostic Systems be liable for indirect, incidental or consequential damages.
No part of this publication may be reproduced, transmitted, transcribed, stored in retrieval systems, or translated into any language or
computer language, in any form or by any means, electronic, mechanical, magnetic, optical, chemical, manual, or otherwise, without the prior
written permission of BD, 7 Loveton Circle, Sparks, Maryland 21152 USA.
BD, the BD Logo, Synapsys, and Veritor are trademarks of Becton, Dickinson and Company or its affiliates. All other trademarks are the
property of their respective owners. © 2022 BD. All rights reserved.
09 2022-02
Updated for IVDR 2017/746 and added Near Patient symbol. Updated Intended Use statement.
Added Safe Disposal statement. Updated technical information, EC REP address and Symbol
Glossary. Added CH REP symbol with address. Updated serious incident statement. Added
Intended User Section and Updated Summary and Explanation Section / Mise à jour de
l'IVDR 2017/746 et ajout du symbole de diagnostic près du patient. Mise à jour de la déclaration
relative à l'application. Ajout de la déclaration relative à la mise au rebut sécurisée. Mise à jour des
informations techniques, de l'adresse du représentant dans la CE et du glossaire des symboles.
Ajout du symbole CH REP avec l'adresse du représentant. Mise à jour de la déclaration relative aux
incidents graves. Ajout de la section Utilisateur et mise à jour de la section Résumé et explication /
Gemäß IVDR 2017/746 aktualisiert und Symbol für patientennahe Tests hinzugefügt. Erklärung zum
Verwendungszweck aktualisiert. Erklärung zur sicheren Entsorgung hinzugefügt. Technische
Informationen, EC-REP-Adresse und Symbolglossar aktualisiert. CH-REP-Symbol mit Adresse
hinzugefügt. Erklärung zu schwerwiegenden Vorkommnissen aktualisiert. Abschnitt „Vorgesehene
Anwender“ hinzugefügt und Abschnitt „Zusammenfassung und Erklärung“ aktualisiert. /
Aggiornamento per IVDR 2017/746 e aggiunta del simbolo "Near patient" (analisi decentrate).
Aggiornamento dell'istruzione sull'uso previsto. Aggiunta dell'istruzione sullo smaltimento sicuro.
Aggiornamento delle informazioni tecniche, dell'indirizzo del mandatario nella Comunità europea
e del glossario dei simboli. Aggiunta del simbolo e dell'indirizzo del mandatario in Svizzera.
Aggiornamento della dichiarazione sugli incidenti gravi. Aggiunta della sezione Utente previsto
e aggiornamento della sezione Riepilogo e spiegazione. / Se ha actualizado para IVDR 2017/746 y
se ha añadido el símbolo de análisis de diagnóstico inmediato. Se ha actualizado la declaración de
uso previsto. Se ha añadido la declaración de eliminación segura. Se ha actualizado la información
técnica, la dirección del representante de la CE y el glosario de símbolos. Se ha añadido el símbolo
del representante de CH y la dirección. Se ha actualizado la declaración de incidentes graves. Se ha
añadido la sección Usuarios previstos y se ha actualizado la sección Resumen y explicación. /
Uppdaterad för IVDR 2017/746 och tillägg av symbolen Produkt för patientnära testning.
Uppdaterade information om avsedd användning. Tillägg av information om säker kassering.
Uppdaterade teknisk information, EC REP-adress och symbolförteckning. Tillägg av CH REP-
symbol med adress. Uppdaterade meddelande om allvarliga incidenter. Tillägg av avsnittet Avsedd
användare och uppdaterade avsnittet Sammanfattning och förklaring
Revision/
Révision/
Version/
Revisione/
Revisión/
Revision
Date/Date/
Datum/Data/
Fecha/Datum
Change Summary/Résumé des modifications/Zusammenfassung der Änderungen/
Riepilogo delle modifiche/Resumen de modificaciones/Sammanfattning av ändringar
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