BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    OZ POWER SYRINGE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Nimbus

    FDA UDI
    Nuvasive, Inc.·00195377055552·Nimbus Adapter, Small Clamp

    SeaSpine Spinous Process System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OHMNISCAN NG

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GYNECARE MESH UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·August 5, 2015

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON INC·Product code OTN·February 21, 2013

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 1, 2014

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·September 24, 2014

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 26, 2015

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 5, 2015