BEUDAMED
    5 results · 38ms · 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 ×

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    UNKNOWN·Product code ITJ·April 16, 2013

    HUDSON NEBULIZER ADAPTER, STERILE, 033

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CAF·March 15, 2011

    ACCU-CHECK AVIVA TEST STIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 17, 2008

    TRILOGY ACETABULAR SYSTEM LINER

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LPH·August 23, 2017

    VERSYS HIP SYSTEM FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·August 23, 2017