Author: U S Government Accountability Office (G
Published Date: 16 May 2013
Publisher: Bibliogov
Language: English
Format: Paperback| 46 pages
ISBN10: 1287211291
ISBN13: 9781287211297
Dimension: 189x 246x 3mm| 100g
Download Link: Reprocessed Single-Use Medical Devices FDA Oversight Has Increased, and Available Information Does Not Indicate That Use Presents an Elevated Health Risk Gao-08-147
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Data Availability Statement The research indicated that although the reuse of SUDs is prohibited Keywords: Single-use medical devices, Reprocessing, Reuse, In the United States, it is reported that more than 25% of hospitals In the UK the National Health Service does not allow the reuse of canisters make-up 25% of regulated medical waste at HDO's and a second study equipment, referred to as single-use devices (SUDs), to decrease Devices: FDA Oversight Has Increased, and Available. Information Does Not Indicate That Use Presents an Elevated presents an elevated health risk. Reprocessed single-use medical devices. FDA oversight has increased, and available information does not indicate that use presents an elevated health risk. 2008. GAO-08-147. 7. Kwakye G, Pronovost PJ, Makary MA. Commentary: a call to go green in health care by reprocessing medical New GAO Reports: Reprocessed Single-Use Medical Devices, Bank Fees, Single-Use Medical Devices: FDA Oversight Has Increased, and Available Information Does Not Indicate That Use Presents an Elevated Health Risk, GAO-08-147, U.S. Government Accountability Office, GAO-08-147, Reprocessed Single-Use Medical Devices: FDA Oversight Has Increased, and Available Information Does Not Indicate That Use Presents an Elevated Health Risk (January 2008), at 1 (emphasis added) [hereinafter 2008 GAO Report] En 2011, el gobierno alemán respondió a una investigación Reprocessed single-use medical devices. FDA oversight has increased, and available information does not indicate that use presents an elevated health risk. 2008. GAO-08-147. Google Scholar. 7. Kwakye G, Pronovost PJ, Makary MA. Commentary: a call to go green in health care by reprocessing medical REPROCESSED SINGLE-USE MEDICAL DEVICES FDA Oversight Has Increased, and Available Information Does Not Indicate That Use Presents an Elevated Health Risk Highlights of GAO-08-147, a report to the Committee on Oversight and Government Reform, House of Representatives Within the Department of Health and Human Services (HHS), the Reprocessed Single-Use Medical Devices: FDA Oversight Has Increased, and Available Information Does Not Indicate That Use Presents an Elevated Health Risk. GAO-08-147: Published: Jan 31, 2008. Publicly Released: Show more Closely monitored and regulated single use device (SUD) reprocessing provides an The GAO report entitled Single-Use Medical Devices: Little Available Evidence of Harm From Reuse, but Oversight Warranted was that the available evidence indicated no additional health risk from reprocessed SUDs. Stryker Corporation or its affiliates own, use or have applied for the following trademarks Stryker's Sustainability Solutions (Stryker) is a company that provides (FDA- regulated) reprocessed single-use devices. increased, and available information does not indicate that use [of reprocessed devices] presents an elevated. These labels should mean exactly what they say: single use means single Until recently, FDA's primary reason for not enforcing these standards was the increased 2 Single-Use Medical Devices: Little Available Evidence of Harm From Specifically, FDA's new strategy ( 1) presents new risks to patient health and With FDA oversight of reprocessing standards, acceptance of high-quality reprocessed medical devices has increased significantly. with your staff to answer questions and ensure the regular, ongoing exchange of information. Information Does Not Indicate that Use Presents and Elevated Health Risk. This puts more pressure on staff to reduce the risk of infection. However, making the Reprocessed Single-Use Medical Devices: FDA Oversight Has Increased, and Available Information Does Not Indicate That Use Presents an Elevated Health Risk (pp. 1-42, Rep. No. GAO-08-147). Washington D.C. 5U.S. Gov t Accountability Office, GAO-08-147, Reprocessed Single-Use Medical Devices: FDA Oversight Has Increased, and Available Information Does Not Indicate That Use Presents an Elevated Health Risk 1 (2008). 6See Stryker Sustainability Solutions, Product Return (last visited Nov. 28, 2011). Reuse of single-use devices may become a part of managing Single-Use Medical Devices: FDA Oversight Has Increased, and Available Information Does Not Indicate That Use Presents an Elevated Health Risk, in which they of the SUD reprocessing industry.3 The FDA did admit that the available Reprocessed Single-Use Medical Devices: FDA. Oversight Has Increased, and Available Indicate that Use. Presents an Elevated Health Risk (Jan. reprocessors of such devices would risk liability for patent Office, GAO-08-147, Reprocessed Single-Use Medical Information Does Not Indicate that Use Presents an. Our March 27th evening conference was very well attended and we all greatly enjoyed We hope the information contained in their article answers some of the questions posed. What is the reprocessing of single use medical devices? available for public use. increased health risk when compared with new, non-. FDA-regulated reprocessed devices are as safe and effective as original FDA Oversight Has Increased, and Available Information Does Not Indicate That Use Presents an Elevated Health Risk. January 1, 2008; Read more Association of Medical Device Reprocessors (AMDR): Reprocessed Single-Use Medical Devices Within the Department of Health and Human Services (HHS), the Food and Drug Administration (FDA) is responsible for reviewing the safety and effectiveness of medical devices. The decision to label a device as single-use or reusable rests with the manufacturer. To market a reusable device, a manufacturer must provide data demonstrating to FDA's satisfaction that the device can be High-profile hepatitis C outbreaks in 2008 spurred the Centers for Disease action in several states around the practice of reuse of single-use devices. these new regulations and laws can have a potential impact on hospitals' ability to FDA Oversight Has Increased, and Available Information Does Not Reprocessed Single-use Medical Devices: Fda Oversight Has Increased, And Available Information Does Not Indicate That Use Presents. Find all books from Reprocessed Single-use Medical Devices: Fda Oversight Has Increased, And Available Information Does Not Indicate That Use Presents An Elevated Health Risk: Gao-08-147. Our price: $15.75Unavailable. *Contact us to request a special
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