BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    BIOSACA SYSTEM, MODEL 800

    FDA 510(k)
    FDA Class 2 ·Neurology

    Monolith

    FDA UDI
    Nuvasive, Inc.·00887517698070·Monolith Core, Ø14x46mm

    Ureteral Stent Systems, Biliary Drainage Catheters

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MODIFICATION TO LUX1540 HANDPIECE AND LUX 1440 HANDPIECE

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

    LUX 1440

    FDA Adverse Event
    Malfunction ·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012

    DEPUY ASR XL FEM IMP SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 6, 2013

    MAXIMO II CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·February 15, 2011

    TRANSVENE RV

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·August 8, 2014

    UNIVERSA FIRM URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·March 26, 2018