According to GlobalData’s medical device pipeline database, eight Peripheral Drug Eluting Stents 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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Of these devices, six are in active development, while the remaining two are in an inactive 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 peripheral drug eluting stent is a mesh-like tube structured thin wire present with a coating of drug or medicine which helps in preventing the arteries from re-stenosis. One unit refers to one peripheral drug eluting stent.
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 Peripheral Drug Eluting 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 Peripheral Drug Eluting Stents devices. Overall, most of these Peripheral Drug Eluting Stents pipeline devices are being developed by private entities.
Key players involved in the active development of Peripheral Drug Eluting Stents include Shenzhen Salubris Pharmaceuticals, University of Pittsburgh, Zylox-Tonbridge Medical Technology, 3D Biotek, Boston Scientific, Cook Medical and HeMo Bioengineering.
For a complete picture of the developmental pipeline for Peripheral Drug Eluting 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.
