BEUDAMED
    4 results · 68ms · 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 ×

    12.5 FR (4.2 MM) (.166 IN.) PEEL-AWAY CATHETER INTRODUCER

    FDA Adverse Event
    Injury ·RAYNHAM·Product code GYK·September 15, 2022

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 27, 2014

    ASR XLA M/L SLEEVE 12/14 +2

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 14, 2012

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·September 8, 2010