BEUDAMED
    30 results · 69ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    8FT PROXENON HEADLIGHT FIBER

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code FST·March 12, 2012

    OJEMAN CORTICAL STIMULATOR

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code GYC·January 10, 2012

    CRW BIOPSY PLUS

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code HAW·February 6, 2013

    XENON LIGHT SOURCE 300 WATT W/

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON MA, INC.·Product code FCW·March 6, 2013

    9300XDP LIGHTSOURCE FAMILY TREE

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code KOG·January 29, 2013

    MLX 300W XENON LIGHTSOURCE

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code FCW·February 11, 2013

    MLX 300W XENON LIGHTSOURCE

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code FCW·March 12, 2014

    ASSY, HEADBAND ULTRALITE 2 BIF

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code FCW·June 14, 2013

    NEUROSIGHT ARC ON LAPTOP

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code HAW·December 5, 2020

    ASSEMBLY, 9300XSP L/S W/AWOS T

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code GCT·July 8, 2014

    CUSA NXT EXTENDED LENGTH TIP, 5 PACK

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA INC.·Product code LFL·August 6, 2014

    UCHR POST, ANTERIOR

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code HAW·August 16, 2012

    OJEMAN CORTICAL STIMULATOR

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code GYC·January 29, 2019

    CUSA EXCEL 23KHZ STANDARDTIP

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code LFL·January 7, 2016

    ULTRALITE PRO MODULE

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code FCW·August 29, 2013

    ASSEMBLY, 9300XSP L/S W/AWOS T

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code FCW·September 17, 2013

    MODEL B 110 V ELECTRO DERMATOME COMPLETE KIT

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code GFD·May 25, 2017

    CRW PRECISION ARC SYSTEM

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code HAW·March 13, 2015

    MLX 300W XENON LIGHTSOURCE

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON, MA, INC.·Product code FCW·January 20, 2015

    CRW PRECISION ARC SYSTEM STERLIZATION CASE

    FDA Adverse Event
    Injury ·INTEGRA BURLINGTON MA, INC·Product code HAW·March 6, 2015