BEUDAMED
    7 results · 28ms · 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 Regulation: Us FDA ×

    MEPILEX

    FDA 510(k)
    FDA Unclassified ·Unknown

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111166785·MICRO NH STR .6MM JAW 6" W/LK

    TEARLAB OSMOLARITY SYSTEM

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    FlareHawk Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FPA·June 27, 2014

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 31, 2013

    UNKNOWN DEPUY 54X36MM METAL LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·January 31, 2011