BEUDAMED
    111 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LANCE DVC

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·October 3, 2019

    INRATIO2

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·June 30, 2010

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·June 30, 2010

    COOLSCULPTING HOLLYWOOD BODY LASER

    FDA Adverse Event
    Injury ·ZELTIQ AESTHETICS INC.·Product code OOK·February 24, 2023

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO·Product code GJS·July 2, 2010

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·July 13, 2010

    INRATIO2

    FDA Adverse Event
    Injury ·BIOSITE INCORPORATED·Product code GJS·June 30, 2010

    DREAMSTNAUTOBIPAPHUMCELL DOM

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·April 12, 2022

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·August 25, 2010

    INRATIO2

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·July 13, 2010

    HALO90 ABLATION CATHETER

    FDA Adverse Event
    Other ·BARRX MEDICAL INC.·Product code GEI·March 11, 2010

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·July 22, 2010

    SURGITEK

    FDA Adverse Event
    Injury ·MEDICAL ENGINEERING CORP.·Product code FTR·June 23, 2000

    REPLICON

    FDA Adverse Event
    Injury ·MEDICAL ENGINEERING CORP.·Product code FTR·May 19, 1995

    MW5076004

    FDA Adverse Event
    Malfunction ·March 22, 2018

    CELSITE

    FDA Adverse Event
    Malfunction ·B.BRAUN MEDICAL SAS·Product code LJT·January 15, 2021

    UTERINE FIBROID MORCELLATOR

    FDA Adverse Event
    Injury ·UNK·Product code GCJ·April 17, 2019

    CASSI II MODEL S BIOPSY DEVICE

    FDA Adverse Event
    Malfunction ·SANARUS TECHNOLOGIES, LLC·Product code KNW·September 29, 2010

    SENOGRAPHE ESSENTIAL MAMMOGRAPHY UNIT

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS SCS·Product code MUE·June 8, 2016

    SOCLEAN 2

    FDA Adverse Event
    Injury ·SOCLEAN, INC.·Product code LRJ·July 10, 2024