4FDA.Enforcement Priorities for Single-Use Devices Reprocessed by Third Parties and Hospitals[EB/OL].[2000-08-14].http://www.fda.gov/Medical Devices/Device Regulationand Guidance/Guidance Documents/ucm107164.htm.
5FDA.Frequently-Asked-Questions about the Reprocessing and Reuse of Single-Use Devices by Third-Party and Hospital Reprocessom[EB/OL].[2001-07-06].http://www.fda.gev/Medical Devices/Device Regulationand Guidance/Guidance Documents/ucm070864.htm.
6FDA.Hospital Reprocessors:Guidance on Adverse Event Reporting for Hospitals that Reprocess Devices Intended by the Original Equipment Manufacturer for Single USe[EB/OL].[2001-04-24].http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm070773.htm.
7FDA.Reprocessing and Reuse of Single-Use Devices:Review Prioritization Scheme[EB/OL].[2000-02-08].http://www.fda.gov/ downloads / Medical Devices / Device Regulationand Guidance/ Guidance Documents/UCM073761.pdf.
8FDA.Medical device user fee modernization Act[S].2002-10-01.
9Popp W,Rasslan O,Unahalekhaka A,et al.What is the use?An international look at reuse of single-use medical devices[J].Int J Hyg Environ Health,2010,213(4):302.
10Roth K,Heeg P,Reichl R.Specific hygiene issues relating to reprocessing and reuse of single-use devices for laparoscopic surgery[J].Surg Endosc,2002,16(7):1 091.
