BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    TUBING, SINGLE USE OXYGEN SUPPLY

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    ILIF

    FDA UDI
    Nuvasive, Inc.·00887517263711·ILIF Trial, 20mm

    Ophthalmic Cannula

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

    Daytona Small Stature

    FDA UDI
    Seaspine Orthopedics Corporation·10889981152642·Fixed Crossbar, 4.5 x 20mm

    The Orthodontic Store

    FDA UDI
    Young Innovations, Inc.·00843471178669·Anatomical Molar Bands, Upper Right 1St & 2Nd M...

    PULSE CARDULE (MODEL 1859/1860 ECG)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PBS MODEL 701A COMPRESSION THERAPY DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·September 26, 2012

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·May 8, 2015

    DURASTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·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