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PUBMED FOR HANDHELDS

Journal Abstract Search


149 related items for PubMed ID: 10109830

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  • 5. SMDA '90 (Safe Medical Devices Act of 1990): user facility requirements of the final medical device reporting regulation.
    Shepherd M.
    J Clin Eng; 1996; 21(2):114-48. PubMed ID: 10155904
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  • 8. Two-page FDA form eases device-act compliance.
    Benson JS.
    Health Facil Manage; 1992 Feb; 5(2):40-7. PubMed ID: 10116138
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  • 11. The Safe Medical Devices Act. What nurses should know about user reporting, implant tracking.
    Koch FA, Solomon RP, Nash SE.
    AORN J; 1992 Feb; 55(2):537-48. PubMed ID: 1536545
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  • 13. Facilities strive to comply with new Act. The long-term effects of the Safe Medical Devices Act are still unknown.
    Schuster DK, Butler KH.
    Health Prog; 1993 May; 74(4):53-7. PubMed ID: 10125364
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  • 14. Proposed FDA "unsafe" lead wire ban could affect many medical devices.
    Hosp Technol Ser; 1995 Jul; 14(7):12-4. PubMed ID: 10144657
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  • 15. Impact of the Safe Medical Devices Act on healthcare facilities.
    Lekhy C.
    J Healthc Qual; 1993 Jul; 15(1):36-8. PubMed ID: 10123341
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  • 18. MedWatch: FDA's new medical products reporting program.
    Kessler DA, Kennedy DL.
    J Clin Eng; 1993 Jul; 18(6):489-92. PubMed ID: 10130858
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  • 19. ANSI/AAMI ES60601-1: A new approach to device standards.
    Schmidt M.
    Biomed Instrum Technol; 2006 Jul; 40(3):246-7. PubMed ID: 16796337
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