According to GlobalData’s medical device pipeline database, five Single Chamber Pacemakers devices are in various stages of development globally. GlobalData’s report Single Chamber Pacemakers 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, four are in active development, while the remaining two are in an inactive stage of development. All devices are in the late stages of development.

Cardiovascular Devices are used to detect and treat heart and circulatory system related diseases. A single chamber pacemaker is a device which has a single pacing lead placed into a chamber of the heart. It is implanted in the chest to help control the heart rate. It has one lead, which is attached to the right ventricle. The pacemaker sends electrical impulses to the heart to keep the ventricle beating at a regular rate.

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 Single Chamber Pacemakers 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 Single Chamber Pacemakers devices. Overall, most of these Single Chamber Pacemakers pipeline devices are being developed by private entities.

Key players involved in the active development of Single Chamber Pacemakers include Boston Scientific, Krisara Engineering, Medtronic, MicroPort CRM and University of Southern California.

For a complete picture of the developmental pipeline for Single Chamber Pacemakers 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.