BEUDAMED
    22 results · 24ms · Sources: EU EUDAMED, US FDA

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    M.U.S.T. MINI POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·August 27, 2025

    MUST MINI POLYAXIAL SCREW 3.5 X 12 FULL THREAD + NUT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·April 6, 2018

    MUST MINI POLYAXIAL SCREW 3.5 X 12 FULL THREAD + NUT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·March 8, 2022

    M.U.S.T. MINI Posterior Cervical Screws System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MUST MINI ROD TI 3.5 X 80MM (STERILE)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·July 13, 2021

    MUST MINI MUST MINI POLYAXIAL SCREW 3.5 X 24 FULL THREAD + NUT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·July 14, 2020

    MUST MINI POLYAXIAL SCREW 3.5 X 18 FULL THREAD + NUT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·October 27, 2022

    MUST MINI ROD REDUCTION DEVICE

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·September 27, 2019

    M.U.S.T. MINI POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·August 11, 2025

    MUST MINI POLYAXIAL SCREW 3.5 X 20 FULL THREAD + NUT

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code KWP·February 2, 2018

    NEURODYN RUBY MUSCLE STIMULATOR, NEURODYN AUSSIE MUSCLE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    THE HELENA V8 IMMUNODISPLACEMENT KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    NEEDLE ECLIPSE 21X1-1/2 RB TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMI·April 21, 2020

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·December 20, 2018

    BD ECLIPSE NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMI·July 7, 2020

    BD NEEDLE ECLIPSE 21X1-1/2 RB TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMI·February 12, 2020

    ASR UNI FEMORAL IMPL SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·June 14, 2013

    ACCOLADE PLUS TMZF HIP STEM #4

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MEH·July 18, 2011

    SILICONE ADVANCED OPTIC-VIOLET SHIELD

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·September 17, 2008

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·April 1, 2019