BEUDAMED
    628 results · 36ms · 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 Status: Malfunction ×

    LIKORALL OVERHEAD LIFT

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FSA·March 3, 2025

    ICT

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS (CLEVELAND), INC.·Product code JAK·May 14, 2018

    SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code MNI·April 21, 2011

    SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC·Product code NKB·September 17, 2015

    LIKORALL 200

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FSA·October 3, 2025

    FIREBIRD SFS

    FDA Adverse Event
    Malfunction ·ORTHOFIX US LLC·Product code LXH·December 17, 2024

    PHOENIX SFS

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code LXH·January 19, 2018

    FIREBIRD SFS

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code LXH·May 4, 2017

    FIREBIRD SFS

    FDA Adverse Event
    Malfunction ·ORTHOFIX MEDICAL INC·Product code NKB·December 4, 2023

    FIREBIRD SFS

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code KWP·May 18, 2018

    FIREBIRD SFS

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code LXH·May 17, 2017

    BLACKSTONE SFS ROD

    FDA Adverse Event
    Malfunction ·BLACKSTONE MEDICAL, INC.·Product code KWQ·October 20, 2005

    PHOENIX SFS SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC·Product code NKB·April 15, 2016

    LIKORALL OVERHEAD LIFT

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FSA·April 7, 2026

    SPINE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC·Product code MNI·September 30, 2015

    SFS SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC·Product code MNH·November 22, 2010

    SFS SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC·Product code MNH·April 11, 2017

    SFS SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC·Product code MNH·April 13, 2017

    SABER RX4MM20CM155

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code LIT·August 26, 2020

    2530088-2013-01183

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code MJO·September 26, 2013