BEUDAMED
    838 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    HARMONIC ACE 5MM SHEAR

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 7, 2020

    ECHELON ENDOPATH STAPLER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 7, 2020

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·January 3, 2020

    ENDOPATH XCEL TROCAR

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·January 7, 2020

    ULTRACISION HARMONIC ACE (EXACT CODE UNKNOWN)

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 21, 2018

    ECHELON ENDOPATH STAPLER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 21, 2018

    UNKNOWN SUNNYVALE PRODUCT

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GEI·May 5, 2015

    STEALTHSTATION S8 PREMIUM SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC·Product code HAW·April 11, 2019

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·August 14, 2018

    MEDTRONIC MCS

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code DSQ·July 8, 2022

    HALO90 ABLATION CATHETER

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GEI·May 22, 2015

    WAVELIGHT FS200 FEMTOSECOND LASER

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code GEX·May 11, 2017

    WAVELIGHT FS200 FEMTOSECOND LASER

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code GEX·May 11, 2017

    INTERPLATE L INTERBODY FUSION DEVICE/VBR

    FDA Adverse Event
    Injury ·RSB SPINE·Product code MAX·May 11, 2010

    INTERPLATE C-TI CERVICAL PLATE/IFD

    FDA Adverse Event
    Injury ·RSB SPINE·Product code KWQ·December 16, 2010

    INTERPLATE L-TI LUMBAR PLATE/IFD/VBR

    FDA Adverse Event
    Injury ·RSB SPINE·Product code KWQ·March 30, 2011

    INTERPLATE CERVICAL TI IFD

    FDA Adverse Event
    Injury ·RSB SPINE·Product code KWQ·July 17, 2009

    INTERPLATE CERVICAL IFD

    FDA Adverse Event
    Injury ·RSB SPINE·Product code OVD·February 2, 2009

    VEGA TOTAL KNEE

    FDA Adverse Event
    Injury ·AESCULAP AG / B. BRAUN·Product code JWH·April 25, 2018

    AGB+

    FDA Adverse Event
    Injury ·ARROW·Product code DQY·February 26, 2014