BEUDAMED
    10,000 results · 77ms · 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 Status: Malfunction ×

    UNKNOWN 3-MM BALL-TIPPED GUIDE WIRE (SGN)

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code DQX·November 22, 2016

    VYSIS LSI MDM2 SPECTRUMORANGE, 20 UL PROBE

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code MVU·June 25, 2020

    PROXIMATE LINEAR STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 22, 2014

    TARGET DEVICE GAMMA3® 300X160MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code HSB·November 22, 2016

    TARGET DEVICE GAMMA3® 300X160MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code HSB·November 22, 2016

    TARGET DEVICE GAMMA3®

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code HSB·November 22, 2016

    STEALTHSTATION S7 SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·February 14, 2017

    TARGET DEVICE GAMMA3® 300X160MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code HSB·November 22, 2016

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CV·Product code GEI·September 14, 2015

    ETHIBOND 2/0 TC D/A 17MM 75CM

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAT·November 6, 2025

    ETHIBOND 2/0 TC D/A 17MM 75CM

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAT·November 6, 2025

    POWERED 60 ECHELON +, 340MM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·April 17, 2023

    LIGACLIP CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·October 27, 2015

    VITEK® 2 GN TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code JTO·November 24, 2015

    VITEK® 2 GRAM-NEGATIVE IDENTIFICATION TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code JTO·December 3, 2015

    VITEK® 2 GRAM-NEGATIVE IDENTIFICATION TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code JTO·September 10, 2015

    VITEK 2 COMPACT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·August 20, 2021

    VITEK® 2 GN ID TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code LQM·September 15, 2017

    VITEK® 2 GRAM-NEGATIVE IDENTIFICATION TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code JTO·September 8, 2015

    VITEK® 2 GN TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code JTO·August 5, 2016