BEUDAMED
    89 results · 45ms · Sources: EU EUDAMED, US FDA

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    ABG I CERAMIC HEAD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·February 3, 2017

    UNKNOWN CERAMIC HEAD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·April 18, 2016

    FABIUS

    FDA Adverse Event
    Malfunction ·DRAEGER MEDICAL, INC.·Product code BSZ·March 30, 2005

    FABIUS

    FDA Adverse Event
    Malfunction ·DRAEGER MEDICAL, INC.·Product code BSZ·June 23, 2005

    FEMORAL HEAD 32MM DIA. -5

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWY·July 20, 2016

    ACCULIS MICROWAVE

    FDA Adverse Event
    Injury ·MICROSULIS MED LTD·Product code GEI·July 21, 2011

    3.5MM 90-S SERFAS ENERGY SUCTION PROBE

    FDA Adverse Event
    Injury ·STRYKER ENDOSCOPY PUERTO RICO·Product code GEI·January 15, 2007

    APEX MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·OMNI LIFE SCIENCE, INC.·Product code KWY·March 18, 2009

    E360 VENTILATOR

    FDA Adverse Event
    Other ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 7, 2009

    DELTA V-40 CERAMIC HEAD 36/+2,5

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LZO·August 2, 2013

    UNKNOWN CERAMIC HEAD 12/14

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWA·June 3, 2016

    ENDOSCOPE SHEATH, REUSABLE

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code HIH·September 1, 2023

    MOSES PULSE

    FDA Adverse Event
    Malfunction ·LUMENIS LTD·Product code GEX·December 23, 2024

    PROFEMUR (L) CLASSIC STEM

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LPH·April 24, 2018

    BIOLOX DELTA PROSTH.HEAD 12/14 36MM M

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code LZO·June 18, 2019

    UNKNOWN V40 HEAD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LZO·June 19, 2018

    PITT EASY ABUTMENT

    FDA Adverse Event
    Injury ·SYBRON IMPLANT SOLUTIONS GMBH·Product code NHA·June 30, 2010

    FABIUS PLUS

    FDA Adverse Event
    Malfunction ·SHANGHAI DRAEGER MEDICAL INSTRUMENT CO. LTD.·Product code BSZ·November 10, 2023

    PERMANENT CAUTERY HOOK INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code GEI·August 6, 2008

    APOLLO

    FDA Adverse Event
    Malfunction ·DRAGER MEDICAL GMBH·Product code BSZ·March 13, 2013