BEUDAMED
    3,933 results · 44ms · 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 ×

    INTEGRIS CATH LAB SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS·Product code IZJ·May 14, 1996

    KODAK X-MATIC ID CAMERA

    FDA Adverse Event
    Malfunction ·EASTMAN KODAK CO.·Product code IZJ·February 15, 2000

    CINE CAMERA - ARRITECHNO CAMERA

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC.·Product code IZJ·December 30, 1992

    ARRITECHNO CINE CAMERA

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code IZJ·March 16, 1998

    ARRITECHNO CINE CAMERA

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code IZJ·March 30, 1998

    SIEMENS

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS·Product code IZJ·December 4, 1998

    BLAZER-C VERTEBRAL AUGMENTATION SYSTEM

    FDA Adverse Event
    Malfunction ·IZI MEDICAL PRODUCTS·Product code OCJ·May 6, 2026

    OSTEO-SITE

    FDA Adverse Event
    Malfunction ·IZI MEDICAL PRODUCTS·Product code DWO·December 3, 2024

    KIVA VCF TREATMENT SYSTEM KIT FIRST FRACTURE- LEFT

    FDA Adverse Event
    Malfunction ·IZI MEDICAL PRODUCTS LLC·Product code NDN·October 14, 2020

    SNAP ON SPHERZ

    FDA Adverse Event
    Malfunction ·IZI MEDICAL PRODUCTS, LLC·Product code HAW·July 12, 2022

    MAMMOTOME DUAL CORE

    FDA Adverse Event
    Malfunction ·IZI MEDICAL PRODUCTS LLC·Product code KNW·October 28, 2024

    SPHERZ PASSIVE REFLECTIVE MARKER

    FDA Adverse Event
    Malfunction ·IZI MEDICAL PRODUCTS INC.·Product code FZZ·November 27, 2007

    BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·IZI MEDICAL PRODUCTS, LLC·Product code KNW·October 25, 2023

    VISICOIL FIDUCIAL

    FDA Adverse Event
    Malfunction ·IZI MEDICAL PRODUCTS LLC·Product code KXK·January 21, 2025

    SHAFT FOR 90 SCREWDRIVER

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXX·September 2, 2020

    1.5MM DIA DRILL BIT W/6MM STOP 13MM LENGTH F/90° SCREWDRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code DZI·August 15, 2014

    Ø1.5MM DRILL BIT W/8MM STOP 15MM F/90° SCRWDRVR MTRXMANDBL

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code DZI·July 13, 2017

    Ø1.5MM DRILL BIT W/8MM STOP 15MM F/90° SCRWDRVR MTRXMANDBL

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code DZI·October 7, 2014

    SCREWHOLDER F/90° SCREWDRIVER WITHOUT INSERT

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HXX·December 3, 2018

    SHAFT FOR 90° SCREWDRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code DZI·September 15, 2014