BEUDAMED
    6 results · 28ms · 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 ×

    TIBIAL BLOCK AND SCREWS PRECOAT SIZE 6 5 MM THICKNESS

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·February 6, 2017

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 21, 2013

    MINICAP DISCONNECT W

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CUERNAVACA·Product code KDI·December 30, 2010

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 18, 2014

    UNKNOWN SHOULDER COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·April 16, 2024

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK ENDOSCOPY·Product code FGE·September 14, 2018