BEUDAMED
    6 results · 35ms · 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 ×

    3.5MM LCP® PROXIMAL HUMERUS PLATE-STANDARD 5H SHAFT/114MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KTW·May 20, 2014

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·November 5, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 23, 2010

    BINAXNOW STREP PNEUMONIAE 12T

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code GTZ·March 27, 2025

    BINAXNOW STREP PNEUMONIAE 12T

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code GTZ·March 27, 2025

    BINAXNOW STREP PNEUMONIAE 12T

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code GTZ·March 27, 2025