According to GlobalData’s medical device pipeline database, 28 Endotracheal Tubes devices are in various stages of development globally. GlobalData’s report Endotracheal Tubes 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, 12 are in active development, while the remaining 16 are in an inactive stage of development. There are 11 products in the early stages of development, and the remaining one is in the late stages of development.

Endotracheal tubes are used to maintain an unobstructed passageway especially to deliver oxygen or anesthesia to the lungs during surgery or any airway management procedure. This curved tube is placed through the patient’s nose or mouth into the trachea (windpipe). One unit refers to one endotracheal tube.

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 Endotracheal Tubes 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 Endotracheal Tubes devices. Overall, most of these Endotracheal Tubes pipeline devices are being developed by private entities.

Key players involved in the active development of Endotracheal Tubes include Allvivo Vascular, Avir Medical, Baylor College of Medicine, Enox Biopharma, Fogless International, Iasis Molecular Sciences, Illumitube, Johns Hopkins University, Laval University and Medical Device Investments.

For a complete picture of the developmental pipeline for Endotracheal Tubes 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.