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

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    MATRIX HA PEEK Cervical IBF System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CLASSIC INTERMITTENT CATHETER

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

    MICROSTAT PVA FOAM EMBOLIZATION PARTICLES

    FDA 510(k)
    FDA Class 2 ·Neurology

    PARIETEX RIGID FOLD PY 14X10 W CUTX1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·November 6, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·July 19, 2011

    GYNECARE PROLIFT +M TOTAL PELVIC FLOOR REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·July 18, 2013

    GEN II RESURF PATELLA 38MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·February 19, 2019

    LEGION CR NP FEM SZ 8 RT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·February 18, 2019