BEUDAMED
    4 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 ×

    RATCHETING ADAPTER, CANNULATED

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code LXH·April 1, 2021

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·June 10, 2014

    ASKU

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DTE·October 9, 2010

    PERMANENT CAUTERY SPATULA

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·December 10, 2012