BEUDAMED
    4 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 ×

    EQUINOXE HUMERAL STEM PRIMARY PRESS FIT 10MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·December 29, 2023

    ASR ACETABULAR IMPLANT 64

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·December 17, 2010

    ARMADA 14 PTA CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LIT·January 29, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 15, 2014