Interventional Cardiology Devices Market Opportunities by Types, Demand, Top Manufactures and Application in Grooming Regions
The global interventional cardiology devices market is expected to
witness considerable growth during the forecast period, owing to the increasing
prevalence of coronary artery disease (CAD), rising geriatric population,
technological advancements in interventional cardiology devices, and growing
demand for non-invasive treatments. Normal balloons, drug-eluting stents,
guiding catheters, embolic protection devices, and vascular closure devices are
different types of devices used in the CAD surgical procedures.
On the basis of product, the interventional cardiology devices market
is categorized into angioplasty balloons, angioplasty stents, catheters, plaque
modification devices, hemodynamic flow alteration, and others. Of these
categories, angioplasty stents dominate the interventional cardiology devices
industry, owing to the increasing demand of different types of stents, such as
drug eluting stents, bare-metal stents, and bioabsorbable stents for the
treatment of CAD. The others category mainly includes guidewires, vascular
closure devices, introducer sheaths, and balloon inflation devices.
The interventional cardiology devices market is bifurcated into
hospitals and ASCs, on the basis of end user. During the historical period,
hospitals category generated the highest revenue in the market, due to the
increased prevalence of CAD along with the increased number of surgical
procedures.
Geographically, North America held the largest share in the
interventional cardiology devices market in 2017, globally, followed by Europe.
The North American market is primarily driven by increasing demand for
interventional cardiology devices, presence of key established players,
developed reimbursement policies, and increasing prevalence of CAD.
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Launch of various advanced interventional cardiovascular devices for
CAD by key players is the major trend observed in the interventional cardiology
devices market. For example, in September 2018, Terumo Corporation launched
Ultimaster Tansei drug-eluting stent in Japan; and in May 2018, the company
launched the product in Europe.
However, high cost of devices, stringent regulatory requirements,
presence of effective first-line treatments can be viewed as restraints
hampering the growth of the interventional cardiology devices market. The
regulatory requirements for the affiliation of medical devices are complex and
undergo amendments with changing needs. These regulations are complicated,
primarily because of the legal aspects associated with them. The quality and
performance of medical devices are necessary facets that need stringent
evaluation to ensure public safety. Thus, complex and stringent standards
followed for the affiliation of medical devices, restrict the growth of the
global market to some extent. Key players in the interventional cardiology devices industry are
introducing new and advanced interventional cardiology devices by seeking
approval from regulatory bodies.
For instance, in September 2018, Biotronik SE & Co. KG received
the United States Food Drug and Administration (USFDA) approval for the PK
Papyrus covered coronary stent system under Humanitarian Device Exemption for
use in the emergency treatment of acute coronary perforations.
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In May 2018, Medtronic plc initiated clinical study in the U.S. to
assess the safety and efficacy of drug-eluting stents bifurcation lesions in
patients with CAD. The data from this study will support an application for an
indication expansion to include bifurcation lesions for the Resolute Onyx
drug-eluting stents from the USFDA.
In May 2018, Abbott Laboratories received approval from the USFDA for
XIENCE Sierra, the newest generation of the company’s XIENCE drug-eluting
stents. This new generation drug-eluting stent system is designed for the
treatment of complex cases, including people with multiple or totally blocked
vessels.
Some of the other players in the global interventional cardiology devices market include Boston
Scientific Corporation, Cardinal Health Inc., B. Braun Melsungen AG, Biotronik
SE & Co. KG, Terumo Corporation, and Biosensors International Group.
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