BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    DISPOSABLE SPINAL INTRODUCER SHEATH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471156050·K-WIRE - SINGLE TROCAR 1.1mm DIA x 230mm

    LIGHTFORCE LF 20/30 980NM SURGICAL DIODE LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ZVPLASTY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    QUINTEX DYNAMIC SCREW 4.0X12MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code KWQ·April 16, 2014

    HEARTSTREAM FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 31, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·December 29, 2010