BEUDAMED
    76 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    DYONICS ACROMIOBLASTER

    FDA Adverse Event
    Injury ·RENOVO, INC.·Product code HRX·May 19, 2026

    DENOVO SPACE MAINTAINER BAND CHAIRSIDE SPACE MAINTAINER

    FDA Adverse Event
    Injury ·DENOVO DENTAL, INC.·Product code ECM·September 1, 2022

    TESERA 3-D PRINTED ALIF CAGE

    FDA Adverse Event
    Injury ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code MAX·July 3, 2018

    A200 KNEE SYSTEM

    FDA Adverse Event
    Injury ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code JWH·September 16, 2016

    A200 KNEE SYSTEM

    FDA Adverse Event
    Injury ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code JWH·September 16, 2016

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·November 7, 2024

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·May 11, 2021

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·March 20, 2023

    THERMOCOOL® SMART TOUCH¿ BI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·March 18, 2024

    IMPELLA 5.5 WITH SMARTASSIST S2 SET, US

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 19, 2026

    SHOCKWAVE IVL SYSTEM WITH THE SHOCKWAVE C2+ CORONARY IVL CATHETER

    FDA Adverse Event
    Injury ·SHOCKWAVE MEDICAL, INC.·Product code QMG·April 24, 2026

    KIT, 14FR INTRODUCER, 13CM&25CM, STERILE

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code DYB·March 3, 2026

    FLEXABILITY¿ ABLATION CATHETER, SENSOR ENABLED¿ CATHETER

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code OAD·January 22, 2024

    PROTEGE EVERFLEX SELF-EXPANDING STENT SYSTEM STANDARD

    FDA Adverse Event
    Injury ·COVIDIEN·Product code FGE·June 24, 2016

    SHOCKWAVE C2 CORONARY INTRAVASCULAR LITHOTRIPSY (IVL) SYSTEM

    FDA Adverse Event
    Injury ·SHOCKWAVE MEDICAL, INC.·Product code QMG·September 18, 2023

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·January 3, 2019

    SHOCKWAVE C2 CORONARY INTRAVASCULAR LITHOTRIPSY (IVL) SYSTEM

    FDA Adverse Event
    Injury ·SHOCKWAVE MEDICAL, INC.·Product code QMG·May 17, 2023

    SHOCKWAVE IVL SYSTEM WITH THE SHOCKWAVE C2+ CORONARY IVL CATHETER

    FDA Adverse Event
    Injury ·SHOCKWAVE MEDICAL, INC.·Product code QMG·April 3, 2026

    SHOCKWAVE C2 CORONARY INTRAVASCULAR LITHOTRIPSY (IVL) SYSTEM

    FDA Adverse Event
    Injury ·SHOCKWAVE MEDICAL, INC.·Product code QMG·July 20, 2023

    SHOCKWAVE C2 CORONARY INTRAVASCULAR LITHOTRIPSY (IVL) SYSTEM

    FDA Adverse Event
    Injury ·SHOCKWAVE MEDICAL, INC.·Product code QMG·January 30, 2024