BEUDAMED
    41 results · 23ms · Sources: EU EUDAMED, US FDA

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    ExactechGPS Total Shoulder Application

    FDA 510(k)
    FDA Class 2 ·Neurology

    ELECTROPHYSIOLOGY SYSTEMS INTEGRATOR (EPSI)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NUVANT, MOBILC CARDIAC TELEMETRY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MYSPINE MC VERTEBRA L04

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code PQC·July 6, 2018

    REDUCTION CANNULATED PEDICLE SCREW 5X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·February 17, 2023

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·March 17, 2020

    MYSPINE S01 DRILL BASED GUIDE

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code PQC·December 12, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 17, 2013

    NC TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·July 23, 2011

    GYNECARE MORCELLEX TISSUE MORCELLATOR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code HET·September 22, 2008

    MYSPINE-MC DRILL GUIDE L03

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PQC·May 26, 2023

    MYSPINE STOPPER SLEEVE 30 MM, DRILL2.7 - LUMBAR

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LXH·February 26, 2020

    IKAZUCHI ZERO

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·June 13, 2019

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·August 19, 2019

    IKAZUCHI ZERO

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·August 20, 2019

    KANEKA PTCA CATHETER CO-R7(IKAZUCHI ZERO)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·August 21, 2019

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·April 14, 2022

    KANEKA PTCA CATHETER CO-R8 (TASUKI)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·December 13, 2020

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·December 21, 2020

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·April 13, 2022