BEUDAMED
    6 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 ×

    NCP BIPOLAR LEAD

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·December 30, 2005

    PASSPORT 2 MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·April 30, 2013

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·August 22, 2014

    EON IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 28, 2011

    PROXIMAL HUMERUS, RIGHT, ÿ 9X160MM

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code HSB·May 14, 2024

    BLUNT TIP SCREW, ÿ 4X40MM

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code HSB·May 14, 2024