BEUDAMED
    11 results · 25ms · 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 ×

    RADIFOCUS OPTITORQUE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·March 7, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014

    UNKNOWN GASTROJEJUNAL FEEDING TUBE

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code KNT·October 28, 2018

    UNKNOWN GASTROJEJUNAL FEEDING TUBE

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code KNT·October 28, 2018

    UNKNOWN GASTROJEJUNAL FEEDING TUBE

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code KNT·October 28, 2018

    UNKNOWN GASTROJEJUNAL FEEDING TUBE

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code KNT·October 28, 2018

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·July 8, 2016

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·July 8, 2016

    OPTITORQUE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·Product code DQO·January 20, 2021