BEUDAMED
    15 results · 27ms · 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 FDA Adverse Event ×

    ENDOCLAMP AORTIC CATHETER

    FDA Adverse Event
    Injury ·HEARTPORT INC.·Product code DWF·August 30, 2001

    ENDOCLAMP AORTIC CATHETER

    FDA Adverse Event
    Injury ·HEARTPORT INC.·Product code DWF·August 30, 2001

    ENDOCLAMP AORTIC CATHETER

    FDA Adverse Event
    Injury ·HEARTPORT INC.·Product code DWF·August 30, 2001

    ENDOCLAMP AORTIC CATHETER

    FDA Adverse Event
    Injury ·HEARTPORT INC.·Product code DWF·August 30, 2001

    IMPELLA 5.5

    FDA Adverse Event
    Malfunction ·ABIOMED, INC.·Product code OZD·September 30, 2024

    XMAX MOTOR

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code ERL·February 14, 2013

    ZOOM CRITICAL CARE BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·February 3, 2011

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 15, 2008

    FEMUR SCREW STD 18MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code OLO·May 31, 2022

    UNKNOWN INTELLIJOINT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code OLO·May 31, 2022

    WALLACH ULTRA FREEZE

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·August 24, 2023

    ARCOS CON SZ A STD 50MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 26, 2023

    ARCOS 15X190MM SPL TPR DIST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 26, 2023

    28MM DIA COCR MOD HD -3MM NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDG·May 26, 2023

    O-ARM O2 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·SANMINA -SCI SYSTEMS·Product code OWB·January 27, 2021