BEUDAMED
    672 results · 39ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GLUMA DESENSITIZER

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH & CO. KG, MEDICAL DIVISION·Product code KLE·August 20, 2013

    IBOND SELF ETCH

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH & CO. KG, MEDICAL DIVISION·Product code KLE·September 17, 2013

    VENUS COMPOSITE

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH & CO. KG, MEDICAL DIVISION·Product code EBF·October 1, 2013

    GLUMA DESENSITIZER

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH & CO. KG, MEDICAL DIVISION·Product code KLE·October 15, 2013

    VENUS COMPOSITE

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH & CO. KG, MEDICAL DIVISION·Product code EBF·October 1, 2013

    GLUMA DESENSITIZER

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH & CO. KG, MEDICAL DIVISION·Product code KLE·October 15, 2013

    GLUMA DESENSITIZER

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH & CO. KG, MEDICAL DIVISION·Product code KLE·October 15, 2013

    GLUMA DESENSITIZER

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH & CO. KG, MEDICAL DIVISION·Product code KLE·October 15, 2013

    VENUS COMPOSITE

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH & CO. KG, MEDICAL DIVISION·Product code EBF·October 1, 2013

    GLUMA DESENSITIZER

    FDA Adverse Event
    Injury ·HERAEUS KUZER GMBH·Product code KLE·March 30, 2007

    GLUMA DESENSITIZER

    FDA Adverse Event
    Injury ·HERAEUS KULZER, HMBH·Product code KLE·June 3, 2011

    VENUS DIAMOND

    FDA Adverse Event
    Injury ·HERAEUS KULZER GUMBH·Product code EBF·August 27, 2013