BEUDAMED
    5 results · 26ms · 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 ×

    LUX 1440

    FDA Adverse Event
    Malfunction ·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012

    DEPUY ASR XL FEM IMP SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 6, 2013

    MAXIMO II CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·February 15, 2011

    TRANSVENE RV

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·August 8, 2014

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·March 26, 2018