ECRI expert reviews reuse of 'single-use medical devices'

Journal of Clinical Monitoring and Computing

Volumn 14, Issue 3, 1998, Pages 203-205

  Solomon, Ronni P ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

COST CONTROL; DISPOSABLE EQUIPMENT; HEALTH CARE COST; INFORMED CONSENT; LEGAL LIABILITY; MALPRACTICE; PRIORITY JOURNAL; RECYCLING; REGULATORY MECHANISM; RISK; SHORT SURVEY;

DISPOSABLE EQUIPMENT; EQUIPMENT REUSE; HUMANS; INFORMED CONSENT; LIABILITY, LEGAL; MALPRACTICE;

EID: 0031835614     PISSN: 13871307     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Short Survey

References (12)

1. ECRI. Special Report on Reuse of Single-Use Medical Devices: Making Informed Decisions. Plymouth Meeting, PA 19462, U.S.A.
2. United States Department of Health and Human Services, U.S. Food and Drug Administration (PDA), Center for Devices and Radiological Health. Devices: reuse of medical disposable devices. In: U.S. Food and Drug Administration. Compliance policy guide 7124.16 § 300.500. Rockville (MD): FDA; reissued September 24,1987
3. 42 CFR § 405.2150
4. 42 CFR § 405.2138 (a)(4)
5. 42 CFR § 405.2139
6. 42 CFR § 405.2136 (b)
7. Schultz WB. Testimony before United States Senate, Committee on Labor and Human Resources, 1996 February
8. Kahan JS, Martin CJ. Extra-label uses of approved drugs. Pharm Exec 1992 April
9. See the discussion at notes 28 to 32 of this chapter
10. Priester R, Caplan A. Legal and ethical issues in the practice of reuse. Perspect Healthc Risk Manage 1991; 11 (4): 31-37
11. Ibid
12. See the discussion in: Lafferty R, Giboffsky A. Regulatory and legal issues in the reprocessing and reuse of hemodialyzers. J Leg Med 1988; 9 (2): 279-311