BEUDAMED
    10 results · 24ms · Sources: EU EUDAMED, US FDA

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    OXIMETER, CO-, IL MODEL 282

    FDA 510(k)
    FDA Class 2 ·Hematology

    ILIF

    FDA UDI
    Nuvasive, Inc.·00887517263353·ILIF Trial, 8mm

    Ophthalmic Cannula

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

    The Orthodontic Store

    FDA UDI
    Young Innovations, Inc.·00843471178430·Anatomical Molar Bands, Upper Right 1St & 2Nd M...

    CAREO SAFETY SYRINGE 1CC/ML, MODELS CA0106-C,CA0196-C,CA0186-C,CA0107-C,CA0197-C,CA0187-C,CA0104-C,CA0194-C,CA0184-C,

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NILE Alternative Fixation Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·April 18, 2014

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·September 20, 2012

    SM PLUS BTT/ROUND BALLOON DISSECTOR

    FDA Adverse Event
    Malfunction ·USSC PUERTO RICO·Product code GCJ·July 12, 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