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

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    DePuy Synthes Porous Polyethylene Implants and Titanium Wires Portfolio – MR Conditional

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MYSPINE MC VERTEBRA L04

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

    NUFACE PLUS

    FDA 510(k)
    FDA Class 2 ·Neurology

    MEDEGEN PRESSURE RATED EXTENSION SETS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    REDUCTION CANNULATED PEDICLE SCREW 5X45

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

    MYSPINE S01 DRILL BASED GUIDE

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

    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

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013

    HUMAPEN MEMOIR

    FDA Adverse Event
    Malfunction ·ELI LILLY AND COMPANY·Product code NSC·July 29, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 18, 2014

    M.U.S.T. MIDLINE CORTICAL (MC) SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·July 16, 2025

    MYSPINE UNILATERAL LEFT GUIDE S01

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code PQC·August 22, 2024

    ENH. POLY-AXIAL PEDICLE SCREW - CANNULATED 5X40MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·January 10, 2024

    BD MAXPLUS PRESSURE RATED EXTENSION SET WITH REMOVABLE NEEDLELESS CONNECTOR

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·June 2, 2023

    BD MAXPLUS PRESSURE RATED EXTENSION SET WITH REMOVABLE NEEDLELESS CONNECTOR

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·June 2, 2023

    M.U.S.T. MIDLINE CORTICAL (MC) SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·December 13, 2024

    MYSPINE MYSPINE MC DRILL BASED GUIDE L04

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PQC·February 14, 2020

    HEARTMATE MOBILE POWER UNIT, NA

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·February 4, 2019