BEUDAMED
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    CADD EXTENSION SETS

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·April 13, 2022

    NEURON DELIVERY CATHETER 053

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·April 13, 2009

    RIA DRIVESHAFT L520

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HTO·March 6, 2014

    SCREWDRIVER BLADE, CANNULATED

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS-FREIBURG·Product code LXH·March 15, 2013

    SAVVY PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·November 20, 2009

    BD SYRINGE 5ML LL 22GA 1-1/4IN PTK 5

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMF·December 16, 2019

    ARTHRODESIS NAIL, LEFT 13 X 700MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·December 1, 2009

    BD MAXGUARD¿ EXTENSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·June 1, 2023

    ABBOTT AXSYM SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·September 30, 2009

    ABBOTT AXSYM SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code LEH·September 30, 2009

    ABBOTT AXSYM SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code LEH·September 30, 2009

    ABBOTT AXSYM SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code LEH·September 30, 2009

    ABBOTT AXSYM SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code LEH·September 30, 2009

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code LXH·January 6, 2011

    RIA 2 REAMING KIT 520MM STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTO·July 5, 2024

    16.5MM REAMER HEAD FOR RIA 2 STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTO·July 5, 2024

    CADD EXTENSION SETS

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·October 21, 2022

    RIA 2 BONE HARVESTING KIT 520MM STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTO·July 5, 2024

    15.5MM REAMER HEAD FOR RIA 2 STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTO·July 5, 2024

    OMNIFIX

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FMF·December 19, 2014