BEUDAMED
    5 results · 18ms · 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 ×

    FLEXIBLE BRONCHOSCOPE

    FDA Adverse Event
    Death ·OLYMPUS·Product code EOQ·September 16, 1994

    RUSCH ENDOTRACHEAL TUBE WITH CUFF

    FDA Adverse Event
    Death ·RUSCH·Product code LNZ·September 16, 1994

    QUADCUT STRAIGHTSHOT

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC·Product code HTT·March 1, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 16, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·August 8, 2014