BEUDAMED
    553 results · 73ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    ABC SELF-LOCKING CERVICAL SCREW 4.0X16MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code KWQ·July 17, 2010

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code MJO·October 26, 2016

    CASPAR DISTR PIN16MMSTER

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LXH·August 21, 2008

    BICONTACT S COCR CEMENTED 12/14 SZ.10MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 5, 2012

    BICONTACT S PLASMAPORE 12/14 SIZE 17MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code JWH·April 27, 2012

    THREADED PIN HEADLESS 3.2MM X 63MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LXH·May 29, 2009

    BICONTACT S COCR CEMENTED 12/14 SZ.16MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code LWJ·April 27, 2012

    BICONTACT PLASMAPORE 12/14 SIZE 17MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 27, 2012

    COLLECT.NO.QAS KNEE IMPLANTS VEGA

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code JWH·December 2, 2016

    ENDURO MENISCAL COMPONENT F2 12MM

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code KRO·November 10, 2016

    ACTIV L INSERTION INSTRUMENT F/H10MM

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code MJO·December 30, 2016

    UNIVATION F MENISCAL COMP.T3 RM/LM 7MM

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code HRY·November 17, 2016

    COLLECT.NO.QAS KNEE IMPLANTS VEGA

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code JWH·October 28, 2016

    EXCIA T PLASMAPORE 12/14 SIZE 15MM

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code LZO·November 10, 2016

    PLASMACUP SC PLASMAPORE-¿CAP SIZE 54MM

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code MEH·October 24, 2016

    TRIAL INSERT I 32MM SYM.

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code HWT·September 29, 2015

    QUINTEX SEMICONSTRAINED SCREW 4.0X16MM

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code KWQ·September 29, 2015

    TRIAL INSERT J 32MM SYM.

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code HWT·September 29, 2015