BEUDAMED
    84 results · 27ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    GMK-SPHERE REVISION FIXED TIBIAL TRAY CEMENTED SIZE 2 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 21, 2019

    BD NEXIVA¿ 24GA 0.75IN Y

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 21, 2018

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 30, 2018

    KYPHON EXPRESS II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code HRX·June 10, 2018

    KYPHON EXPRESS¿ II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·January 20, 2022

    KYPHON® EXPRESS¿ II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO S. DE R.L DE C.V.·Product code HRX·November 28, 2018

    HUDSON VOLDYNE 2500 VOLUMETRIC EXCERCISER

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BWF·May 14, 2013

    SEE H-10

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code HQL·September 26, 2014

    ADAPTA SR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NVZ·June 14, 2011

    KYPHON EXPRESS II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code HRX·June 29, 2018

    KYPHON EXPRESS II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code HRX·June 29, 2018

    KYPHON® EXPRESS¿ INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·April 25, 2017

    KYPHON EXPRESS INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·October 17, 2017

    KYPHON EXPRESS INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·October 17, 2017

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 4/10MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 14, 2018

    KYPHON® EXPRESS¿ II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·July 11, 2018

    KYPHON EXPRESS INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·March 14, 2018

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 3/20MM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code JWH·April 8, 2016

    KYPHON EXPRESS II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·January 9, 2018

    ARTHROSCOPE

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·March 28, 2019