209 related articles for article (PubMed ID: 10175836)
21. The potential impact of usp general chapter <797> on procedures and requirements for the preparation of sterile radiopharmaceuticals.
Hung JC
J Nucl Med; 2004 Jun; 45(6):21N-6N. PubMed ID: 15181115
[No Abstract] [Full Text] [Related]
22. Reconciliation of FDA and societal guidelines for endoscope reprocessing.
Alvarado C
Gastrointest Endosc Clin N Am; 2000 Apr; 10(2):275-81. PubMed ID: 10683214
[TBL] [Abstract][Full Text] [Related]
23. Examining the new AAMI standard...containment devices for reusable medical device sterilization.
Larrick K;
Biomed Instrum Technol; 2007; 41(2):155-6. PubMed ID: 17432671
[No Abstract] [Full Text] [Related]
24. Device design with reprocessing in mind.
Asa R
Mater Manag Health Care; 1994 May; 3(5):44-6, 48, 50. PubMed ID: 10133837
[No Abstract] [Full Text] [Related]
25. Reusing medical devices. Ensuring safety the second time around.
Lewis C
FDA Consum; 2000; 34(5):8-9. PubMed ID: 11590804
[No Abstract] [Full Text] [Related]
26. Impact of FDA policy change on the reuse of single-use medical devices in Michigan hospitals.
Alfa MJ; Castillo J
Am J Infect Control; 2004 Oct; 32(6):337-41. PubMed ID: 15454891
[TBL] [Abstract][Full Text] [Related]
27. Outsourcing reusables. Moving device sterilization outside the walls.
OR Manager; 1996 Jun; 12(6):17-9. PubMed ID: 10157854
[No Abstract] [Full Text] [Related]
28. Implementing AORN recommended practices for sterilization.
Graybill-D'Ercole P
AORN J; 2013 May; 97(5):521-33. PubMed ID: 23622825
[TBL] [Abstract][Full Text] [Related]
29. Reuse of single-use medical devices.
Fielder JH
IEEE Eng Med Biol Mag; 1999; 18(6):80-1. PubMed ID: 10576078
[No Abstract] [Full Text] [Related]
30. Requiem for reuse of single-use and reusable devices?
Daschner F
Infect Control Hosp Epidemiol; 2002 Jul; 23(7):356; author reply 357. PubMed ID: 12138969
[No Abstract] [Full Text] [Related]
31. AAMI advice on reprocessing instructions.
OR Manager; 2005 Apr; 21(4):10. PubMed ID: 15999440
[No Abstract] [Full Text] [Related]
32. Federal regulation of single-use medical devices: a revised FDA policy.
Smith JJ; Agraz JA
Food Drug Law J; 2001; 56(3):305-16. PubMed ID: 11944641
[No Abstract] [Full Text] [Related]
33. Report device failures to the FDA.
JCAH Perspect; 1987; 7(7-8):5-7. PubMed ID: 10289785
[No Abstract] [Full Text] [Related]
34. Doubt and proof: the need to verify the cleaning process.
Azizi J; Basile RJ
Biomed Instrum Technol; 2012; Suppl():49-54. PubMed ID: 22559777
[No Abstract] [Full Text] [Related]
35. Reprocessing single-use devices--regulatory roles.
Dunn D
AORN J; 2002 Jul; 76(1):100-6, 108-12, 114 passim; quiz 129-32. PubMed ID: 12134397
[TBL] [Abstract][Full Text] [Related]
36. Patient safety alert. Joint Commission issues patient safety goals.
Hosp Case Manag; 2002 Oct; 10(10):suppl 3-4. PubMed ID: 12325455
[No Abstract] [Full Text] [Related]
37. Sterilization vs. disinfection vs. clean.
Alvarado CJ
Nurs Clin North Am; 1999 Jun; 34(2):483-91. PubMed ID: 10318736
[TBL] [Abstract][Full Text] [Related]
38. Debate on reuse of "disposable" medical equipment fueled by FDA.
Gibson NK
J Clin Monit Comput; 1998 Jan; 14(1):75. PubMed ID: 9641860
[No Abstract] [Full Text] [Related]
39. Cleaning instructions for use: a central sterile service department perspective.
Klacik S
Biomed Instrum Technol; 2012; Suppl():80-4. PubMed ID: 22559783
[No Abstract] [Full Text] [Related]
40. Hospitals' reused tools: reassessing the risk to you.
Hawkins D
US News World Rep; 1999 Nov; 127(21):74. PubMed ID: 10724808
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
