BEUDAMED
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    REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150782·K-WIRE - SINGLE TROCAR 2.5mm DIA x 230mm

    MODEL 486-01 PACING LEAD

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    LIQUI-URA TOXIC URINE CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    PROCEED VENTRAL PATCH

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·January 3, 2013

    HEART START XL

    FDA Adverse Event
    Malfunction ·AGILENT TECHNOLOGIES, INC.·Product code MKJ·November 3, 2010

    PULSAVAC PLUS WOUND DEBRIDEMENT SYSTEM FAN

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code FQH·January 21, 2014