BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    LO-PRO SCRW TM SS 2.7X 14MMCORTEX

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·July 14, 2023

    ST FRANCIS HSP TULSA OK 1

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code DTZ·December 18, 2012

    LO-PRO LOCK SCRW,SS 2.7X 14MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWC·June 6, 2024

    SYMBIQ DCHANNEL 3.01

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·April 10, 2014

    EON MINI 16-CHANNEL IPG

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·October 13, 2010

    ENDURANT II ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·December 20, 2012

    LO-PRO SCRW TM,SS 3.5X 14MMCORT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·July 14, 2023

    LO-PRO SCRW TM,SS 3.5X 18MMCORT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·July 14, 2023

    CLAV FRAC PLT,CENTRAL THIRD,LFT,SS

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·August 15, 2023

    LO-PRO LOCK SCRW,SS 3.5X 14MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·August 4, 2023

    LO-PRO SCRW TM,SS 3.5X 16MMCORT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·July 14, 2023