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

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    IMPRESSION MATERIAL, TRIFLEX SILICONE

    FDA 510(k)
    FDA Class 2 ·Dental

    Ceramill® Zolid

    FDA UDI
    Amann Girrbach AG·E4947602401·

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110553·COAXIAL IRRIGAT-ASPIRAT TIP STR 0.3 PORT

    Daytona Small Stature

    FDA UDI
    Seaspine Orthopedics Corporation·10889981152741·Fixed Crossbar, 4.5 x 40mm

    Straumann ZOLID-HT

    FDA UDI
    Amann Girrbach AG·E494760240STM1·

    K-JUMP DIGITAL THERMOMETER WITH BATTERY-LESS PATCH, MODEL KD-2100

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Perimeter Otis™ 1.0 Optical Coherence Tomography System

    FDA 510(k)
    FDA Class 2 ·Radiology

    SHUNT, CENTRAL NERVOUS SYSTEM & COMPS

    FDA Adverse Event
    Malfunction ·Product code JXG·April 19, 2014

    ENDO SHEARS 5MM INSTRUMENT

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY USSC·Product code GEI·September 20, 2012

    TENDRIL SDX

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·July 16, 2010

    Armada 35/ Armada 35 LL PTA Catheters. The device is intended for dilatation of lesions in the vasculature.

    FDA Enforcement
    Class II ·Terminated·Abbott Vascular·October 3, 2012