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 ×

    WIKTOR PRIME STENT DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC INTERVENTIONAL VASCULAR·Product code MAF·May 6, 1998

    WIKTOR PRIME DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC INTERVENTIONAL VASCULAR·Product code MAF·May 6, 1998

    WAVEWRITER ALPHA? PRIME

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 28, 2026

    DEXTRUS 4137

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·April 29, 2013

    DUROM ACETABULAR COMPONENT

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWA·April 28, 2011

    KINETRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·July 24, 2008