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

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    CERVICAL MUCOUS ASPIRATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902140873·Pediatric Two-Lumen Central Venous Catheterizat...

    I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    IQPACS

    FDA 510(k)
    FDA Class 2 ·Radiology

    LARIAT SUTURE DELIVERY DEVICE

    FDA Adverse Event
    Injury ·SENTREHEART INC.·Product code GAT·February 8, 2013

    PARALLAX ACRYLIC RESIN WITH TRACERS- TA

    FDA Adverse Event
    Other ·ARTHROCARE CORPORATION·Product code NDN·January 7, 2011

    LARGE SUTURECUT NEEDLE DRIVERINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 28, 2014