BEUDAMED
    3 results · 27ms · 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 ×

    PUMP IN STYLE ORIGINAL BREAST PUMP

    FDA Adverse Event
    Malfunction ·MEDELA, INC.·Product code HGX·February 14, 2014

    SHERPA BALANCED 6F GUIDE CATHETER

    FDA Adverse Event
    Injury ·MEDTORNIC, INC·Product code DQY·October 23, 2012

    MAGIC 3 FEMALE INTERMITTENT CATHETER

    FDA Adverse Event
    Malfunction ·ROCHESTER MEDICAL CORP·Product code KOD·May 27, 2015