About the Cuviva Corporation
Cuviva is a Medical Device company
Cuviva AB
Cuviva operates within the business areas Cuviva Medical and Cuviva Communications. Corporate business support functions are shared between the business areas, e.g. finance, marketing, quality, information security, and internal IT. These shared areas of the management systems are certified to the Quality Management System Standards ISO 9001 and the Information Security Management System Standards ISO 27001.
Cuviva has implemented and certified a management system to comply with the regulatory requirements on the markets where we operate. We hold the following certificates:
ISO 13485:2016 Quality Management System
ISO 27001:2022 Information Security System
ISO 14001:2015 Environmental Management System
The Cuviva RPM Platform is CE marked as a class IIa medical device according to the MDR 2017/745.
No parts of the Cuviva website may be reproduced, in any form or by any means, without permission in writing from Cuviva AB, Sweden. However, any person is hereby authorized to copy, print and distribute any document published by Cuviva on the cuviva.com website provided that:
a reference to cuviva.com is made when the document is used
the document is used for information purposes only
the document is used for non-commercial purposes only
Information on this server is provided “as is” without any warranty of any kind, either express or implied, including but not limited to, the implied warranties of merchantability, fitness for a particular purpose, or non-infringement. The information herein may include technical inaccuracies or typographical errors. Changes may periodically be made to the information and will be incorporated in new editions. Cuviva AB may make improvements or changes in products described at any time without notice.
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If you have any questions, please feel free to contact Cuviva at one of the addresses listed on the Contact page.