BEUDAMED
    994 results · 43ms · Sources: EU EUDAMED, US FDA

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    INTELLIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·June 3, 2022

    PCA KNEE

    FDA Adverse Event
    Injury ·HOWMEDICA, INC.·Product code JWH·September 25, 1995

    2GX

    FDA Adverse Event
    Injury ·TISPORT, LLC·Product code IOR·June 27, 2019

    2GX

    FDA Adverse Event
    Injury ·TISPORT, LLC·Product code IOR·August 16, 2018

    2GX

    FDA Adverse Event
    Injury ·TISPORT, LLC·Product code IOR·January 10, 2019

    TILITE 2GX

    FDA Adverse Event
    Injury ·TISPORT, LLC·Product code IOR·November 30, 2021

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE (SGJ)·Product code FRN·September 17, 2008

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE (SGS)·Product code FRN·October 31, 2002

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LMH·June 9, 2011

    DUODOPA_DUOPA

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·April 21, 2021

    DUODOPA_DUOPA

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·December 9, 2024

    TILITE 2GX SERIES 2

    FDA Adverse Event
    Malfunction ·TISPORT, LLC·Product code IOR·August 11, 2016

    SEPRAFILM

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code MCN·April 3, 2023

    J NEEDLE 8G X 4"

    FDA Adverse Event
    Other ·POPPER PRECISION INSTRUMENTS·Product code GDM·December 5, 2001

    8G X 12 MAMMOTOMESTEREOTACTIC PROBE

    FDA Adverse Event
    Malfunction ·DEVICOR MEDICAL PRODUCTS INC·Product code KNW·August 6, 2018

    8G X 12 MAMMOTOMESTEREOTACTIC PROBE

    FDA Adverse Event
    Malfunction ·DEVICOR MEDICAL PRODUCTS, INC.·Product code KNW·July 8, 2019

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·UNKNOWN MANUFACTURING FACILITY·Product code KDJ·August 10, 2010

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·November 20, 2010

    8G X 12 MAMMOTOME STEREOTACTIC PROBE

    FDA Adverse Event
    Malfunction ·DEVICOR MEDICAL PRODUCTS INC·Product code KNW·August 6, 2018

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·November 21, 2017