BEUDAMED
    1,094 results · 28ms · Sources: EU EUDAMED, US FDA

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    CAPD PRIZM

    FDA Adverse Event
    Injury ·SIMS MEDICAL SYSTEMS·Product code FRN·May 21, 2001

    REMSTAR AUTO A-FLEX

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·July 1, 2024

    UNKNOWN SOLITAIRE

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. D/B/A EV3 NEUROVASCULAR·Product code NRY·July 6, 2022

    REBAR

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. D/B/A EV3 NEUROVASCULAR·Product code KRA·July 6, 2022

    TECNIS SYMFONY

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code POE·September 10, 2019

    TECNIS SYMFONY TORIC

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code POE·September 10, 2019

    REFLEX CATHETER

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·February 21, 2023

    CELLO BALLOON GUIDE CATHETER

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·January 17, 2023

    CELLO BALLOON GUIDE CATHETER

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·February 21, 2023

    SOLITAIRE FR

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·January 17, 2023

    SOLITAIRE AB STENT

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NJE·January 17, 2023

    PLATE, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·April 8, 2015

    PLATE, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·April 8, 2015

    ENDEAVOR RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·November 15, 2017

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·November 15, 2017

    ENDEAVOR RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·November 15, 2017

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·November 15, 2017

    UNKNOWN ACTIVE ARTICULATION FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 15, 2018

    UNKNOWN MAGNUM SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·June 25, 2018

    RESOLUTE ONYX RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·June 14, 2018