BEUDAMED
    49 results · 35ms · Sources: EU EUDAMED, US FDA

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    MACOPRODUCTIONS S.A.S.

    FDA registration
    MACOPRODUCTIONS S.A.S.·4 products·🇫🇷 France

    LEVCOREDUCTION FILTER

    FDA Adverse Event
    Malfunction ·MACOPRODUCTIONS S.A.S.·Product code MAC·July 9, 2004

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·July 3, 2013

    FOLFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·February 4, 2013

    UNKNOWN_KNEE

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·June 19, 2024

    Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.

    FDA Enforcement
    Class II ·Terminated·Teleflex Medical·March 7, 2018

    RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM (UNI)

    FDA Adverse Event
    Injury ·MAKO SURGICAL·Product code NPJ·November 1, 2012

    TIBIAL INLAY IMPACTOR HEAD

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code NPJ·January 3, 2019

    ARROW

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL, INC. (SUBSIDIARY OF TELEFLEX, INC.)·Product code DYB·December 2, 2019

    ANSPACH® EMAX2 PLUS MOTOR

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·July 12, 2019

    RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MAKO SURGICAL·Product code NPJ·May 18, 2012

    REAMER HANDLE OFFSET

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·February 20, 2026

    UNKNOWN_MAKO_PRODUCT

    FDA Adverse Event
    Injury ·MAKO SURGICAL CORP.·Product code JWH·June 30, 2015

    RIO® DRAPE KIT-ONE PIECE WITH POCKETS-

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·May 2, 2019

    UNKNOWN MAKO RESTORIS MCK FEMORAL COMPONENT SIZE 2

    FDA Adverse Event
    Injury ·MAKO SURGICAL CORP.·Product code MBH·June 4, 2025

    RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MAKO SURGICAL·Product code NPJ·June 21, 2012

    RESTORIS MULTICOMPARTMENTAL KNEE PROSTHESIS

    FDA Adverse Event
    Injury ·MAKO SURGICAL·Product code NPJ·April 15, 2014

    RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MAKO SURGICAL·Product code NPJ·September 27, 2013

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code KGE·December 14, 2021

    RESTORIS MULTICOMPARTMENTAL PROSTHESIS

    FDA Adverse Event
    Injury ·MAKO SURGICAL·Product code NPJ·February 26, 2014