These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

217 related articles for article (PubMed ID: 6749000)

  • 21. 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]  

  • 22. Guidance on the new packaging standard.
    Flexible Packaging Association
    Med Device Technol; 2006; 17(9):34-5. PubMed ID: 17240685
    [TBL] [Abstract][Full Text] [Related]  

  • 23. FDA guidelines for endoscope reprocessing.
    Cornelius MJ
    Gastrointest Endosc Clin N Am; 2000 Apr; 10(2):259-64. PubMed ID: 10683212
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The Safe Medical Devices Act of 1990--FDA. Notice.
    Fed Regist; 1991 Apr; 56(66):14111-3. PubMed ID: 10111151
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Ethylene oxide, ethylene chlorohydrin, and ethylene glycol: proposed maximum residue limits and maximum levels of exposure.
    Fed Regist; 1978 Jun; 43(122):27473-83. PubMed ID: 10236750
    [No Abstract]   [Full Text] [Related]  

  • 26. Manufacturers of medical devices join the chorus of regulatory critics.
    Stein J
    Natl J (Wash); 1980 Sep; 12(38):1566-9. PubMed ID: 10298001
    [No Abstract]   [Full Text] [Related]  

  • 27. New questions on low-temperature sterilization.
    OR Manager; 1996 Jun; 12(6):16. PubMed ID: 10157853
    [No Abstract]   [Full Text] [Related]  

  • 28. Medical devices; preemption of state product liability claims--FDA. Proposed rule.
    Fed Regist; 1997 Dec; 62(239):65384-8. PubMed ID: 10176832
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Medical devices; current good manufacturing practice (CGMP) final fule; quality system regulation--FDA. Final rule.
    Fed Regist; 1996 Oct; 61(195):52602-62. PubMed ID: 10168287
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Physicochemical, toxicological and hygienic aspects of ethylene oxide application for the sterilization of medical products. III. Setting hygienic norms in sterilized medical products.
    Lyarsky PP; Gleiberman SYe ; Likhtman TV; Kopylova LS; Zayeva GN; Yurchenko VV; Kolesnikova NI; Kareev NV
    J Hyg Epidemiol Microbiol Immunol; 1988; 32(3):257-64. PubMed ID: 3198908
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Exposure of hematopoietic stem cells to ethylene oxide during processing represents a potential carcinogenic risk for transplant recipients.
    Butterworth BE; Chapman JR
    Regul Toxicol Pharmacol; 2007 Dec; 49(3):149-53. PubMed ID: 17761374
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Revised standards for sterilisation: the changes.
    Hoxey E; Strain P; Harries J; Kirk B
    Med Device Technol; 2007; 18(2):33-8. PubMed ID: 17494499
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Voluntary consensus standards and the FDA's regulatory program.
    Gardner S
    Med Instrum; 1979; 13(4):239-42. PubMed ID: 470665
    [No Abstract]   [Full Text] [Related]  

  • 34. Working draft of the FDA GMP final rule (Part II).
    Donawa ME
    Med Device Technol; 1995 Nov; 6(9):9-12. PubMed ID: 10158131
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Enforcement policy: recalls (including product corrections)--guidelines on policy, procedures, and industry responsibilities.
    Fed Regist; 1978 Jun; 43(117):26201-21. PubMed ID: 10316619
    [No Abstract]   [Full Text] [Related]  

  • 36. Medical devices and the US Food and Drug Administration: regulating the tools of radiology.
    Henderson JA; Smith JJ
    J Am Coll Radiol; 2005 Jun; 2(6):504-10. PubMed ID: 17411867
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Medical devices; procedures for premarket notification, premarket approval, classification, performance standards establishment, banning devices, and availability of regulatory hearings--FDA. Final rule.
    Fed Regist; 1992 Dec; 57(238):58400-6. PubMed ID: 10123143
    [TBL] [Abstract][Full Text] [Related]  

  • 38. FDA modernization act of 1997: guidance on medical device tracking; availability--FDA. Notice.
    Fed Regist; 1998 Mar; 63(42):10640-1. PubMed ID: 10177505
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Ethylene oxide sterilization of medical devices: a review.
    Mendes GC; Brandão TR; Silva CL
    Am J Infect Control; 2007 Nov; 35(9):574-81. PubMed ID: 17980234
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Technology assessment of medical devices at the Center for Devices and Radiological Health.
    Kessler L; Richter K
    Am J Manag Care; 1998 Sep; 4 Spec No():SP129-35. PubMed ID: 10185989
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.