BEUDAMED
    3 results · 23ms · 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 ×

    OXF PKS ANAT MEN BRG UHMWPE RT SML SZ 3

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·June 12, 2014

    PFC*SIGMA/OV DOME PAT 3 PEG,32

    FDA Adverse Event
    Injury ·DEPUY (IRELAND)·Product code JWH·December 12, 2012

    EON MINI IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·September 29, 2010