BEUDAMED
    16 results · 20ms · Sources: EU EUDAMED, US FDA

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    POWERED PATIENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BD PLASTIPAK CONCENTRIC LUER LOCK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·February 5, 2019

    SAGICO OSI Spinal System by Osimplant

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    XTRACTOR, MODEL M143

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LINER: MPACT FLAT PE HC LINER Ø36/E

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·December 27, 2019

    MPACT 3D METAL ACETABULAR SHELL Ø52 TWO-HOLE

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·July 5, 2023

    AMISTEM H FEMORAL CEMENTLESS STEM SIZE 6 LAT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KXA·April 28, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC., USA·Product code LFR·October 9, 2007

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·October 31, 2012

    1.5MM TI ORBITAL RIM PLATE 12 HOLES

    FDA Adverse Event
    Malfunction ·SYNTHES ELMIRA·Product code JEY·July 14, 2017

    VANGUARD 360 TIBIAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2018

    BIOMET ARCOM PATELLA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2018

    VANGUARD POSTERIOR STABILIZED FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2018

    VANGUARD POSTERIOR STABILIZED TIBIAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2018

    VANGUARD TIBIAL CRUCIATE WING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·April 19, 2018

    Nikon Metrology XTH cabinet x-ray Systems which includes variations STH225, XTH225ST, and MCT225.

    FDA Recall
    Terminated ·Nikon Metrology·Product code RCE·December 23, 2019