BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Unclassified ·Unknown

    Artman Instruments

    FDA UDI
    Wise Linkers, LLC·D1272423831·Nance Orthodontic Loop Forming Pliers ARTMAN

    MLKJ

    FDA UDI
    Weifang Mingliang Electronics Co., Ltd.·06974077940023·

    THERAPY ABLATION CATHETER

    FDA Adverse Event
    Malfunction ·IRVINE BIOMEDICAL, A ST. JUDE MEDICAL COMPANY·Product code OAD·June 25, 2010

    RSA-CMS

    FDA 510(k)
    FDA Class 2 ·Radiology

    Optima XR200amx, Optima XR220amx

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 2, 2025

    NXSTAGE SYSTEM ONE

    FDA Adverse Event
    Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·November 21, 2008

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 10, 2011

    DOUBLEAIRHOSE F/MINI AIR DRILL NO. 512.1

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·July 23, 2013