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    Norfolk Medical Products, Inc.

    Manufacturer
    🇺🇸 United States

    NORFOLK MEDICAL PRODUCTS, INC.

    FDA registration
    NORFOLK MEDICAL PRODUCTS, INC.·4 products·🇺🇸 United States

    CLEARVIEW

    FDA Adverse Event
    Malfunction ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·September 11, 2003

    CLEARVIEW

    FDA Adverse Event
    Malfunction ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·September 11, 2003

    FUBCUTANEOUS PORT TUBING

    FDA Adverse Event
    Malfunction ·NORFOLK MEDICAL PRODUCTS, INC.·March 7, 1994

    IMPLANTED PORT

    FDA Adverse Event
    Injury ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·January 25, 1995

    OMEGA PORT

    FDA Adverse Event
    Injury ·NORFOLK MEDICAL PRODUCTS, INC.·Product code MDV·October 20, 1994

    OMEGAPORT. SR

    FDA Adverse Event
    Injury ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·April 18, 1997

    OMEGAPORT

    FDA Adverse Event
    Malfunction ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·April 13, 1997

    CATH, OMEGA PORT 9.6 FR

    FDA Adverse Event
    Injury ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·July 20, 1998

    NORPORT SINGLE LUMEN PORT

    FDA Adverse Event
    Malfunction ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·May 7, 2019

    NORPORT SINGLE LUMEN PORT

    FDA Adverse Event
    Malfunction ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·May 7, 2019

    VORTEX PORT

    FDA Adverse Event
    Injury ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·June 5, 1998

    VORTEX PORT

    FDA Adverse Event
    Injury ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·June 4, 1998

    OMEGA PORT-SR ACCESS SYSTEM

    FDA Adverse Event
    Malfunction ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·September 8, 1995

    NORPORT SINGLE LUMEN PORT

    FDA Adverse Event
    Malfunction ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·January 9, 2020

    OHMEGA PORT

    FDA Adverse Event
    Injury ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·February 25, 1998

    BETAPORT ACCESS SYSTEM

    FDA Adverse Event
    Injury ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·October 22, 1997

    TITAN PORT

    FDA Adverse Event
    Injury ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·October 21, 1998

    TITAN PORT

    FDA Adverse Event
    Injury ·NORFOLK MEDICAL PRODUCTS, INC.·Product code LJT·May 28, 1998