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Journal Abstract Search

357 related items for PubMed ID: 7550495

  • 1. Designing medical devices for conformance with harmonized standards. The European Community's Medical Devices Directives and their effect on the product development process.
    Fries RC, Graber MD.
    Biomed Instrum Technol; 1995; 29(4):284-92. PubMed ID: 7550495
    [Abstract] [Full Text] [Related]

  • 2. Designing medical devices for conformance with harmonized standards: a case study of non-active implants.
    Gogins JA.
    Biomed Instrum Technol; 1995; 29(4):294-7. PubMed ID: 7550496
    [Abstract] [Full Text] [Related]

  • 3. The challenges and opportunities of creating an integrated global market for medical devices.
    Higson G.
    Biomed Instrum Technol; 1995; 29(5):441-4. PubMed ID: 7496412
    [No Abstract] [Full Text] [Related]

  • 4. FDA use of international standards in the premarket review process.
    Rechen E, Barth DJ, Marlowe D, Kroger L.
    Biomed Instrum Technol; 1998; 32(5):518-26. PubMed ID: 9800008
    [Abstract] [Full Text] [Related]

  • 5. Early experience of the European Medical Devices Vigilance System.
    Randall H.
    Australas Phys Eng Sci Med; 1997 Dec; 20(4):203-6. PubMed ID: 9503691
    [Abstract] [Full Text] [Related]

  • 6. Medical device regulation for manufacturers.
    McAllister P, Jeswiet J.
    Proc Inst Mech Eng H; 2003 Dec; 217(6):459-67. PubMed ID: 14702983
    [Abstract] [Full Text] [Related]

  • 7. User reporting of medical device related incidents.
    Sievänen H.
    Med Device Technol; 2003 May; 14(4):26-9. PubMed ID: 12774575
    [Abstract] [Full Text] [Related]

  • 8. Update on the European database.
    Donawa M.
    Med Device Technol; 2001 Oct; 12(8):21-4. PubMed ID: 12938545
    [Abstract] [Full Text] [Related]

  • 9. European Community Medical Device Directives.
    Health Trends; 1992 Oct; 24(1):6-7. PubMed ID: 10171283
    [No Abstract] [Full Text] [Related]

  • 10. Regulation of medical devices in the European Union.
    Chai J.
    J Leg Med; 2000 Dec; 21(4):537-56. PubMed ID: 11194571
    [No Abstract] [Full Text] [Related]

  • 11. Human factors in the design of medical devices - Approaches to meeting international standards in the European Union and USA.
    Privitera MB, Evans M, Southee D.
    Appl Ergon; 2017 Mar; 59(Pt A):251-263. PubMed ID: 27890135
    [Abstract] [Full Text] [Related]

  • 12. The European legislation on medical devices.
    Anselmann N.
    Stud Health Technol Inform; 1996 Mar; 28():5-12. PubMed ID: 10172825
    [Abstract] [Full Text] [Related]

  • 13. European directives on medical devices.
    Ludgate SM, Potter DC.
    BMJ; 1993 Aug 21; 307(6902):459-60. PubMed ID: 8400924
    [No Abstract] [Full Text] [Related]

  • 14. The biological evaluation of medical devices used in dentistry. The influence of the European Union on the preclinical screening of dental materials.
    Schmalz G, Browne RM.
    Int Dent J; 1995 Aug 21; 45(4):275-8. PubMed ID: 7558367
    [Abstract] [Full Text] [Related]

  • 15. Materials vigilance and traceability.
    Tracol P.
    Orthop Traumatol Surg Res; 2016 Feb 21; 102(1 Suppl):S95-103. PubMed ID: 26822532
    [Abstract] [Full Text] [Related]

  • 16. How are medical devices regulated in the European Union?
    French-Mowat E, Burnett J.
    J R Soc Med; 2012 Apr 21; 105 Suppl 1(Suppl 1):S22-8. PubMed ID: 22508970
    [No Abstract] [Full Text] [Related]

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  • 19. CE marking and medical device directives.
    Shedden DJ.
    Commun Dis Public Health; 1999 Jan 21; 2(1):73. PubMed ID: 10462905
    [No Abstract] [Full Text] [Related]

  • 20. [Comments and suggestions on the medical device standardization system from the view point of medical devices test].
    Yang X, Wang C, Yang Z, Li D.
    Sheng Wu Yi Xue Gong Cheng Xue Za Zhi; 2013 Jun 21; 30(3):546-51. PubMed ID: 23865316
    [Abstract] [Full Text] [Related]

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