BEUDAMED
    36 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    UNKNOWN DEPUY HV CEMENT

    FDA Adverse Event
    Injury ·DEPUY CMW 9610921·Product code LOD·May 12, 2014

    1818910-2022-08536

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·May 10, 2022

    EON MINI IPG, 16-CHANNEL RECHARGEABLE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 29, 2019

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·November 22, 2021

    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·December 22, 2017

    1.5T LINX, 15B

    FDA Adverse Event
    Injury ·TORAX MEDICAL, INC.·Product code LEI·April 17, 2023

    LAMITRODE 4 LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·March 8, 2012

    EON MINI, SCS IPG

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 23, 2013

    EON MINI IPG, 16-CHANNEL RECHARGEABLE

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 8, 2012

    BRANEMARK SYSTEM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·August 28, 1996

    ETHICON VICRYL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·November 2, 1995

    UNKNOWN DEPUY HV CEMENT

    FDA Adverse Event
    Injury ·DEPUY CMW ¿ REG. # 9610921·Product code LOD·May 12, 2014

    COMPREHENSIVE REVERSE SHOULDER HUMERAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PAO·October 12, 2017

    COMPREHENSIVE REVERSE SHOULDER HUMERAL TRAY W LOCKING RING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 12, 2017

    COMPREHENSIVE REVERSE SHOULDER FIXED LOCKING SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 12, 2017

    COMPREHENSIVE REVERSE SHOULDER CENTRAL SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·October 12, 2017

    COMPREHENSIVE REVERSE SHOULDER FIXED LOCKING SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 12, 2017

    COMPREHENSIVE REVERSE SHOULDER FIXED LOCKING SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 12, 2017

    M2A 38MM MOD HD -6MM NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·February 5, 2020

    M2A 38MMX48MM CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 5, 2020