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2020-03-13
789
Global
Reprocessing is a regulated activity for manufacturing the medical devices that are conducted by third party or hospitals. The US Food and Drug Administration (FDA) requires third-party reprocessors to meet the same standards as originally manufactured single-use devices. Reprocessing is a common practice in the U.S. after the advent of “Honor Roll”, where hospitals were supposed to choose to reprocess single-use devices and 77% of Practice Greenhealth Award winners in 2010 chose to reprocess medical devices with a combined savings of over USD 10.8 million. “Superbug” is the antibiotic resistance that is said to be associated with drug only while the medical device is equally responsible for it. Around 45% of hospitals had agreements with third-party reprocessing companies which increased to 70% in 2008 after the economic recession in the U.S.
Goldstein Market Intelligents analyst forecast the Medical Device Reprocessing market size is growing at a CAGR of 15% through the forecast years (2017-2030). Currently, most hospitals and healthcare facilities outsource Medical Device Reprocessing to qualified third party service providers.
By Device Type
By Product Type
By End User
Based on Geography
Based on geography, North America dominated the global Medical Device Reprocessing market with the market share of 42% in 2017 followed by Europe owing to Directive 93/42/EEC concerning medical devices and distinguishes between reusable devices and those intended for single use, according to which for the reusable medical devices, the manufacturer must provide information on the appropriate process to allow reuse, including cleaning, disinfection, and packaging and, where appropriate, the method of sterilization to be used, and any restriction on the number of reuses. APAC tends to be the fastest growing reprocessed medical device market and Japan, China, Australia, Korea, Indonesia, and India owing to encouraging regulatory policies and rising pressure to keep healthcare budgets under control are expected to fuel the growth of the Medical Device Reprocessing market in the APAC.
According to our global market study on the basis of extensive primary and secondary research: “One trend is partnering with the vendor in order to understand and buy the reprocess medical devices. While the vendor community is divided about the benefits of reprocessing devices, many product vendors and consultancies offer services to assist hospitals in reprocessing and reusing devices.”
Based on geography, North America dominated the global Medical Device Reprocessing market with the market share of 42% in 2017 followed by Europe owing to Directive 93/42/EEC concerning medical devices and distinguishes between reusable devices and those intended for single use, according to which for the reusable medical devices, the manufacturer must provide information on the appropriate process to allow reuse, including cleaning, disinfection, and packaging and, where appropriate, the method of sterilization to be used, and any restriction on the number of reuses. APAC tends to be the fastest growing reprocessed medical device market and Japan, China, Australia, Korea, Indonesia, and India owing to encouraging regulatory policies and rising pressure to keep healthcare budgets under control are expected to fuel the growth of the Medical Device Reprocessing market in the APAC.
According to the report, major driving factor for Medical Device Reprocessing market is the cost saving attribute of reprocessed devices and solutions which is responsible for potential annual savings of USD 2 billion in U.S. health care system from reprocessing and repurchasing 2% of all medical devices and potential cost savings of almost 50% and annual savings of USD 213K by one health system from purchasing Medical Device Reprocessing while Stryker Sustainability Solutions works with hospitals that save over USD 1 million annually as a result of a reprocessing program.
Further, the report states the major challenge is that reprocessing is complex and technical, and it raises concerns about patient safety, ethics, the environment, and costs. Risks of the reprocessed devices outweigh the benefits and that research has not proven it to be safe.
The report covers the present ground scenario and the future growth prospects of the Medical Device Reprocessing market for 2017-2030 along with the data of shipments of Medical Device Reprocessing centers worldwide. We calculated the market size and revenue share on the basis of revenue generated from major players across the globe. We have forecasted the market on the basis of the number of clinics, hospitals, specialty centers and medical labs and the average number of installments of the reprocessed devices in the facilities.
Our global Medical Device Reprocessing Market report comprises of the following companies as the key players:
The study was conducted using an objective combination of primary and secondary information including inputs from key participants in the industry. The report contains a comprehensive market and vendor landscape in addition to a SWOT analysis of the key vendors.
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