BEUDAMED
    226 results · 42ms · Sources: EU EUDAMED, US FDA

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    OPTOMONITOR 3

    FDA Adverse Event
    Malfunction ·OPSENS INC.·Product code DXO·April 19, 2024

    OPTOWIRE DEUX

    FDA Adverse Event
    Malfunction ·OPSENS INC.·Product code DXO·January 20, 2017

    OPTOWIRE DEUX

    FDA Adverse Event
    Malfunction ·OPSENS INC.·Product code DXO·June 11, 2019

    OPTOWIRE DEUX

    FDA Adverse Event
    Malfunction ·OPSENS INC.·Product code DXO·June 10, 2019

    OPTOWIRE DEUX

    FDA Adverse Event
    Injury ·OPSENS INC.·Product code DXO·June 10, 2019

    OPTOWIRE

    FDA Adverse Event
    Malfunction ·OPSENS INC·Product code DQX·January 24, 2023

    OPTOWIRE DEUX

    FDA Adverse Event
    Injury ·OPSENS INC.·Product code DXO·November 18, 2016

    OPTOWIRE DEUX

    FDA Adverse Event
    Injury ·OPSENS INC.·Product code DXO·October 25, 2016

    SAVVYWIRE

    FDA Adverse Event
    Death ·OPSENS INC.·Product code DQX·March 28, 2025

    OLSEN ELECTROSURGICAL INC.

    FDA Adverse Event
    Malfunction ·OEI·Product code GEI·August 23, 1999

    PROXIMATE RELOADABLE LINEAR STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY - ALB·Product code GAG·July 21, 1998

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·March 7, 2011

    ENDOPATH ETS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY·Product code KOG·August 18, 1998

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP·Product code DTQ·October 14, 2011

    DUAL COOLER/HEATER

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWC·July 28, 2011

    FLEX 60 ENDO LINEAR CUTTER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GDW·October 2, 2007

    ENDOPATH ETS

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY·Product code KOG·February 15, 2001

    LIGASURE V SEALER/DIVIDER

    FDA Adverse Event
    Malfunction ·VALLEYLAB·Product code GEI·February 23, 2007

    CT GAMMA DIALYZER (CT 190G)

    FDA Adverse Event
    Malfunction ·NIPRO CORPORATION·Product code FJI·August 8, 2002

    MESH - COMPOSIX KUGEL

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·June 26, 2007