BEUDAMED
    5 results · 20ms · 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 ×

    SELOX SR 53

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code LWS·June 14, 2006

    APEXPLUS

    FDA Adverse Event
    Other ·SUMMIT TECHNOLOGY·Product code LZS·March 16, 2001

    UNKNOWN ZIMMER HIP

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDI·February 6, 2013

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·December 7, 2010

    PRIMEADVANCED

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 22, 2014