BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Transcutaneous Electronic Nerve Stimulator (KTR-2301, KTR-2302, KTR-2341, KTR-2342, KTR-2401, KTR-2402, KTR-2411, KTR-2412, KTR-2491, KTR-2492, KTR-2493, KTR-2494)

    FDA 510(k)
    FDA Class 2 ·Neurology

    Artman Instruments

    FDA UDI
    Wise Linkers, LLC·D1272423321·Dental Automatic Crown Remover Bridge Remover w...

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111138126·BEEBEE CROWN SCISS SH STR 4"

    THERAPY ABLATION CATHETER

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

    TITANIUM TELEGRAPH HUMERAL NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BT-400

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ONE TOUCH ULTRASMART METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·November 21, 2008

    COULTER® PREPPLUS

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JQW·September 10, 2011

    GREENFIELD?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - CORK·Product code DTK·July 23, 2013