According to GlobalData’s medical device pipeline database, five Venous Stents devices are in various stages of development globally. GlobalData’s report Venous Stents 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 six devices of this category are in active stage of development. There are three products in the early stages of development, and the remaining three are in the late stages of development.
A venous stent is a self-expandable metallic stent with perforated tube which is inserted into a vein to prevent the blood flow constriction caused by obstructions and occlusions in the venous vasculature. Venous stent placement is considered in case of significant stenosis or extrinsic compression. Venous stents placed in the iliofemoral vein have been tracked in this market. One unit of venous stent refers to one venous stent system.
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 Venous Stents 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 Venous Stents devices. Overall, most of these Venous Stents pipeline devices are being developed by private entities.
Key players involved in the active development of Venous Stents include Shanghai MicroPort Endovascular MedTech Group, Venous Stent, W. L. Gore & Associates, Zhejiang Kindly Medical Devices and Zylox-Tonbridge Medical Technology.
For a complete picture of the developmental pipeline for Venous Stents 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.
