BEUDAMED
    5 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 ×

    ELLUME COVID-19 HOME TEST

    FDA Adverse Event
    Malfunction ·ELLUME LIMITED·Product code QKP·December 20, 2021

    QUICK-CORE ULTRASOUND BIOPSY NEEDLE

    FDA Adverse Event
    Injury ·COOK ENDOSCOPY·Product code FCG·September 4, 2018

    PROTECTA XT DR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·March 21, 2013

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011

    APR HIP SYSTEM ENHANCED-ACETABULAR INSERT

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code KWB·March 14, 2008