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

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    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·June 15, 2021

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OZO·September 6, 2019

    M2A MODULAR HEAD COMPNOENT 38MM HEAD DIAMETER STANDARD NECK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 13, 2017

    PROMUS ELEMENT? PLUS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 11, 2013

    SIGMA STAB GVF INS 5 8MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC·Product code JWH·July 7, 2011

    HARMONIC ACE 36 CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·September 8, 2008

    M2A 38MM MOD HD STD NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 26, 2018

    M2A-38 CUP 50MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 26, 2018

    MALLORY/HEAD ALTERNATE BEARING SHELL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWZ·February 8, 2017

    M2A MODULAR HEAD COMPONENT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWY·February 8, 2017

    M2A 38 MM ONE-PIECE CUP 38MM X 52 O.D.

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·September 30, 2016

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 4, 2016

    M2A MODULAR HEAD COMPONENT 32MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWY·February 3, 2015

    M2A TAPER LINER 32MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWY·February 3, 2015

    GMK-HINGE FEMORAL COMPONENT SIZE 2 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·June 28, 2019

    GMK-HINGE FIXED TIBIAL INSERT SIZE 1/26MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·July 12, 2019