Hemoglobin assay for validation and quality control of medical device reprocessing

Author:

Frey Justin,Guan Allan,Li Zhenyu,Turtil Steven,Phillips K. Scott

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry,Analytical Chemistry

Reference16 articles.

1. Condon L (2011) Challenges with reprocessing reusable instrumentation. http://www.fda.gov/downloads/MedicalDevices/NewsEvents/WorkshopsConferences/UCM268690.pdf . Accessed 10 June 2015

2. Sheela A (2014) Reprocessed medical devices market expected to reach USD 2.58 billion globally in 2020—transparency market research. In: GlobeNewswire News Room. http://globenewswire.com/news-release/2014/09/17/666582/10098979/en/Reprocessed-Medical-Devices-Market-Expected-to-Reach-USD-2-58-Billion-Globally-in-2020-Transparency-Market-Research.html . Accessed 16 Jan 2015

3. Schaefer MK, Jhung M, Dahl M, Schillie S, Simpson C, Llata E, Link-Gelles R, Sinkowitz-Cochran R, Patel P, Bolyard E, Sehulster L, Srinivasan A, Perz JF (2010) Infection control assessment of ambulatory surgical centers. JAMA 303:2273–2279. doi: 10.1001/jama.2010.744

4. FDA Safety Communication: design of endoscopic retrograde cholangiopancreatography (ERCP) (2015) Duodenoscopes may impede effective cleaning. United States food and drug administration. http://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm434871.htm . Accessed 2 Jun 2015

5. Association for the advancement of medical instrumentation (2011) TIR30:2011: A compendium of processes, materials, test methods, and acceptance criteria for cleaning reusable medical devices. Association for the advancement of medical instrumentation, Fairfax

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