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

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    COOLIEF Cooled Radiofrequency Kit

    FDA 510(k)
    FDA Class 2 ·Neurology

    LINK Instruments - Saw and drill guides

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575397723·Orthopaedic implant aiming/guiding block, reusa...

    FORYOU NPWT DEVICE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BETA-POWDER

    FDA 510(k)
    FDA Class 2 ·Dental

    CARELINK

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

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 11, 2013

    ASR ACETABULAR CUPS 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·July 8, 2011

    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
    Injury ·COOK INC·Product code FAD·June 14, 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