According to GlobalData’s medical device pipeline database, eight Atrial Septal Defect Occluders devices are in various stages of development globally. GlobalData’s report Atrial Septal Defect Occluders 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 three are in an inactive stage of development. There are one products in the early stages of development, and the remaining five are in the late stages of development.
The atrial septal defect occluder is delivered to the heart via cardiac catheter and guidewire. The device releases a self-expandable nitinol mesh which prevents blood flow through the atrial hole. Over time, heart tissue develops over the nitinol mesh to fully occlude the defect. One unit refers to one atrial septal defect occluder implant.
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 Atrial Septal Defect Occluders 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 Atrial Septal Defect Occluders devices. Overall, most of these Atrial Septal Defect Occluders pipeline devices are being developed by private entities.
Key players involved in the active development of Atrial Septal Defect Occluders include Occlutech International, Vascular Closure Systems, atHeart Medical, Carag, Endomimetics, Ension and Lepu Scientech Medical Technology (Shanghai).
For a complete picture of the developmental pipeline for Atrial Septal Defect Occluders 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.
