BEUDAMED
    11 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA × Status: Malfunction × Clear all

    AVANTAGE INLAY SIZE 50/28

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LPH·December 15, 2016

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·October 10, 2014

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·June 11, 2013

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·June 25, 2019

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·June 25, 2019

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·June 26, 2019

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·December 31, 2019

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·December 31, 2019

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·June 26, 2019

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·July 23, 2019

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·August 27, 2019