BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    AVANCE CS2

    FDA Adverse Event
    Injury ·DATEX-OHMEDA, INC.·Product code BSZ·March 25, 2022

    BEI BEI KN95

    FDA Adverse Event
    Injury ·BEI BEI SAFETY CO LTD.·Product code MSH·April 30, 2020

    BEI MEDICAL SYSTEMS CO

    FDA Adverse Event
    Injury ·BEI MEDICAL SYSTEMS CO.·Product code MND·October 30, 2002

    MEDITRON

    FDA Adverse Event
    Injury ·BEI MEDICAL SYSTEMS·Product code FDF·November 17, 1997

    TLIF-C EI 9MM 8DEG 32/10

    FDA Adverse Event
    Injury ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code MAX·January 5, 2024

    TLIF-C EI H 9MM 0DEG 32/10

    FDA Adverse Event
    Injury ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code MAX·February 28, 2020

    CANTOR TUBE

    FDA Adverse Event
    Injury ·WILLY RUSCH AG·Product code FEI·August 27, 1998

    COUPLER, ZOOM, HD, C-MOUNT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code FEI·May 15, 2019

    RVSCH

    FDA Adverse Event
    Injury ·RUSCH INC.·Product code FEI·July 6, 1999

    STERIS SYSTEM 1E

    FDA Adverse Event
    Injury ·STERIS CANADA CORPORATION·Product code MED·February 8, 2017

    MARKED SPRING TIP GUIDEWIRE

    FDA Adverse Event
    Injury ·CONMED CORPORATION·Product code KNQ·May 27, 2014