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

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    MAMMARY SIZER, MAMMARY PROTHESIS SIZER

    FDA 510(k)
    FDA Unclassified ·Unknown

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984106·anteriors; shade A3; mould D 68

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150737·K-WIRE - SINGLE TROCAR 1.0mm DIA x 150mm

    INRATIO PT/INR TEST STRIPS

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·June 21, 2016

    DRAKE WILLOCK REVERSE OSMOSIS WATER TREATMENT SYST

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

    SUPERVISORY TELEMETRY ARRHYTHMIA TERMINAL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·February 28, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·February 10, 2011

    SUPER SUCKER SHORT CURVED (BX/20)

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code KDC·December 18, 2013

    BLADE GUIDE SLEEVE FOR TROCHANTERIC FIXATION NAILS

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code FZX·March 10, 2014

    BLADE GUIDE SLEEVE FOR TROCHANTERIC FIXATION NAILS

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code FZX·January 11, 2016

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·January 8, 2021