BEUDAMED
    7,523 results · 28ms · Sources: EU EUDAMED, US FDA

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    LOCKING SCREW, FULLY THREADED T2 TIBIA Ø5X35 MM

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·April 4, 2019

    LONG NAIL KIT R1.5, TI, LEFT GAMMA3® Ø10X280MM X 130°

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·April 4, 2019

    LOCKING SCREW, FULLY THREADED T2 TIBIA Ø5X37,5 MM

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·April 4, 2019

    END CAP, STD, TI GAMMA3®

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·April 4, 2019

    U-BLADE SET, TI 10.5X95MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·March 27, 2012

    U-BLADE SET, TI 10.5X105MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 6, 2011

    U-BLADE SET, TI GAMMA3 Ø10.5X95MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code HSB·May 15, 2015

    HYPODERMIC NEEDLE-PRO FIXED NEEDLE INSULIN SYRINGE

    FDA Adverse Event
    SMITHS MEDICAL ASD, INC·Product code FMF·January 7, 2013

    U-BLADE SET, TI GAMMA3® Ø10.5X85MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code HSB·October 17, 2014

    GROSHONG 9.5 FR D/L CATHETER

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code DQO·June 4, 1998

    NEED PRODUCTION OF U-500 SYRINGE

    FDA Adverse Event
    Other ·Product code FMF·April 21, 2009

    U-BLADE SET, TI GAMMA3® Ø10.5X80MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code HSB·August 8, 2014

    MEDLINE

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, LP·Product code DXN·May 3, 2026

    U-BLADE SET, TI ? 10.5X100MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·December 22, 2008

    PFC MODULAR KNEE SYSTEM TIBIAL INSERT

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON PROFESSIONAL INC.·Product code HSH·November 20, 1996

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Malfunction ·ALCON-IRVINE TECHNOLOGY CENTER·Product code HQE·April 26, 2006

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES, INC.·Product code HQE·December 3, 1998

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·July 7, 2023

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES(USA)·Product code HWC·April 30, 2014

    OMNIPOD 5 PODS

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code QFG·May 12, 2025