According to GlobalData’s medical device pipeline database, five Percutaneous Ventricular Assist Devices devices are in various stages of development globally. GlobalData’s report provides an overview of the segment’s pipeline landscape and offers detailed analysis of its products. Buy the report here.

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All five devices of this category are in active stage of development. There are three products in the early stages of development, and the remaining two are in the late stages of development.

A Percutaneous Ventricular Assist Device (PVAD) is a catheter-based pump that is placed into the heart to assist in improving cardiac output to meet the oxygen demand of the body. This device utilizes a minimally invasive approach for insertion. One unit refers to one Percutaneous Ventricular Assist Device pump.

Innovations in the medical devices sector are linked to the development of new approaches, processes, or technologies for treating, diagnosing, and managing disease in response to demand from healthcare for better patient outcomes and reduce healthcare costs.

Based on an analysis of GlobalData’s Medical Intelligence Center pipeline product database, these actively developed Percutaneous Ventricular Assist Devices pipeline devices are all expected to be approved within the next ten years.

Currently, private organizations, public entities and institutions are working on the development of Percutaneous Ventricular Assist Devices devices. Overall, most of these Percutaneous Ventricular Assist Devices pipeline devices are being developed by private entities.

Key players involved in the active development of Percutaneous Ventricular Assist Devices include Cardiovascular Systems, Fengkaili Medical Devices (Shanghai), Lifeshield Medical, PulseCath and Suzhou Xinling Med Medical Technology.

For a complete picture of the developmental pipeline for Percutaneous Ventricular Assist Devices devices, buy the report here.

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article. 

The medical devices pipeline data used in this article were obtained from the Medical Pipeline Products Database of GlobalData’s Medical Intelligence Center. The Pipeline Products database is a is a comprehensive source of information on medical devices, it covers 39K products which are in development stage and intended for diagnosis, treatment, and management of diseases/conditions/symptoms directly or indirectly. The pipeline products included in the database are sourced from reliable and authenticated sources, such as company websites, SEC filings, conference presentations, analyst presentations, news releases, clinical trial registries, and grants. The information is collected by following systematic research techniques and proprietary methodology.