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

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    BOEING, POSITIVE AIRWAY PRESSURE (PAP) THERAPY DEVICE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PROCARE

    FDA UDI
    DJO, LLC·00888912038416·SECURE-ALL BODY BELT, 12 PACK

    Astraguard

    FDA UDI
    S D I DIAGNOSTICS INC·B279S297991300·Bacterial viral filter

    MectaLock Ti Suture Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079

    FDA 510(k)
    FDA Class 2 ·Dental

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·March 6, 2013

    MINICAP EXTEND LIFE PD TRANSFSET W/TWIST CLAMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·February 15, 2011

    VERSA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·August 8, 2014

    TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811

    FDA Recall
    Terminated ·Tekia, Inc.·Product code HQL·September 29, 2015

    TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile. The firm name on the label is TEKIA, INC., Irvine, CA.

    FDA Recall
    Terminated ·Tekia, Inc.·Product code HQL·November 9, 2018