BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    PARACENTESIS CATHETER DEVICE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122994·K-WIRE - SINGLE TROCAR 1.4mm DIA x 150mm

    NEURO VISION RADIOGRAPHIC X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    TITAN GEL REP CPK-12 HV

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ZONA PLUS

    FDA Adverse Event
    Injury ·ZONA HEALTH·Product code BXB·March 25, 2013

    SYMBIQ DUAL CHANNEL

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·February 19, 2013

    STRATA II VALVE, REGULAR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·August 1, 2014

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011