BEUDAMED
    619 results · 22ms · Sources: EU EUDAMED, US FDA

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    GDX VCC WITH ECC SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    DR 14S G DX-D IMAGING PACKAGE

    FDA UDI
    AGFA·05414904222218·

    CHOLESTECH GDX

    FDA Adverse Event
    Injury ·INVERNESS MEDICAL·Product code LCP·January 21, 2009

    GDX VCC

    FDA Adverse Event
    Injury ·CARL ZEISS MEDITEC INC·Product code JXE·April 29, 2005

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·December 12, 2012

    Cholestech GDX A1C Test Cartridge. The Cholestech GDX A1C Test is an in-vitro diagnostic test that measures hemoglobin A1c (HbA1c).

    FDA Recall
    Terminated ·Cholestech Corp·Product code LCP·August 3, 2006

    SCALPEL, SAFETY #11, SS, STERIL

    FDA Adverse Event
    Other ·MEDLINE INDUSTRIES, INC.·Product code GDX·January 19, 2009

    SAFETY SCALPEL WITH POLYMER COATED SURGICAL BLADE

    FDA Adverse Event
    Malfunction ·SOUTHMEDIC INC·Product code GDX·September 22, 2015

    MEDLINE

    FDA Adverse Event
    Injury ·MEDLINE·Product code GDX·November 15, 2017

    CARBON STEEL SAFETY SCALPEL #23

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GDX·April 27, 2021

    DEROYAL SAFETY SCALPEL COMPONENT OF TRAY

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL·Product code GDX·April 24, 2012

    SAFETY SCALPEL

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code GDX·June 29, 2012

    COLD KNIFE STRAIGHT BLADE

    FDA Adverse Event
    Malfunction ·CIRCON ACMI·Product code GDX·March 6, 2002

    COLD KNIFE, STRAIGHT BLADE

    FDA Adverse Event
    Malfunction ·ACMI NORWALK·Product code GDX·July 22, 2003

    COLD KNIFE, STRAIGHT BLADE

    FDA Adverse Event
    Malfunction ·ACMI NORWALK·Product code GDX·September 10, 2003

    SAFETY SCALPEL, #11 500/CASE, 500/DOUBLE POLYBAG

    FDA Adverse Event
    Malfunction ·S&S SURGICAL PRODUCTS INC·Product code GDX·August 9, 2024

    ELITE & USA COLD KNIFE, STRIAGHT BLADE, 3/PKG

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code GDX·October 13, 2009

    ETHICON ENDO-SURGERY, LLC

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GDX·October 29, 2009

    MEDLINE

    FDA Adverse Event
    Other ·MEDLINE INDUSTRIES, INC.·Product code GDX·September 10, 2004

    SCALPEL,SAFETY,SS,DISPOSABLE,STERILE

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES INC.·Product code GDX·December 14, 2017