BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    AL-3300

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471156036·K-WIRE - SINGLE TROCAR 0.9mm DIA x 230mm

    PROXIMATE ILS CIRCULAR STAPLERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KOG·June 13, 2006

    BATTERY POWERED PATIENT LIFT

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Hi-Torque Command 14 ST Guide Wire and Hi-Torque Command 14 MT Guide Wire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SILICONE IA TIP, DISPOSABLE

    FDA Adverse Event
    Injury ·ALCON PRECISION DEVICE - SINKING SPRING·Product code HQC·June 30, 2014

    QUATTRODE

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 30, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·December 22, 2010