According to GlobalData’s medical device pipeline database, 29 PTCA Standard Balloon Catheters 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, 11 are in active development, while the remaining 18 are in an inactive stage of development. There are three products in the early stages of development, and the remaining eight are in the late stages of development.
PTCA Standard Balloon Catheters are coronary catheters equipped with a balloon capable of expanding. These balloons may be used alone or in combination with stenting for pre-dilation and post-dilation to achieve optimal stent expansion. They may also be used to predilate arteries prior to PTCA Drug Coated Balloon intervention. One unit refers to one PTCA Standard Balloon Catheter.
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.
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Based on an analysis of GlobalData’s Medical Intelligence Center pipeline product database, these actively developed PTCA Standard Balloon Catheters 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 PTCA Standard Balloon Catheters devices. Overall, most of these PTCA Standard Balloon Catheters pipeline devices are being developed by private entities.
Key players involved in the active development of PTCA Standard Balloon Catheters include SIS Medical, Terumo Aortic, MicroPort Scientific, CorNova, Innovia, iVascular SLU, Medix Innovators, 3DT Holdings, Andramed and Atrium Medical.
For a complete picture of the developmental pipeline for PTCA Standard Balloon Catheters 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.
