BEUDAMED
    29 results · 20ms · Sources: EU EUDAMED, US FDA

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    EagleRay Long Sheath, 0.088 ID, 80cm, 90cm, 100cm and 110cm Lengths, EagleRay Access Catheter, 0.071 ID, 137cm Length, EagleRay Access Catheter, 0.055 ID, 137cm Length, EagleRay Access Catheter, 0.045 ID, 144cm Length, EagleRay Access Catheter, 0.035 ID, 158cm Length

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PedFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361034919·Remind Quad Solid 6.5x50

    PedFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361034872·Remind Quad Solid RBM 6.5x30

    PedFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361034889·Remind Quad Solid 6.5x35

    PedFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361034865·Remind Quad Solid 6.5x30

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361022077·Remind Quad Solid RBM 6.5x55

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014225·Remind Quad Solid RBM 6.5x45

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014218·Remind Quad Solid RBM 6.5x40

    PedFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361034896·Remind Quad Solid 6.5x40

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014201·Remind Quad Solid RBM 6.5x35

    PedFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361034902·Remind Quad Solid 6.5x45

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361022084·Remind Quad Solid 6.5x55

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014232·Remind Quad Solid RBM 6.5x50

    HEARTSTRING III PROXIMAL SEAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DURASPAN HEMODIALYSIS LONG-TERM CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BD MICRO-FINE¿ PRO PEN NEEDLES 32G X 4MM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·June 22, 2023

    BD MICRO-FINE¿ PRO PEN NEEDLES 32G X 4MM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·June 22, 2023

    PEDFUSE

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC·Product code MNI·October 17, 2017

    PEDFUSE

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC·Product code MNH·October 13, 2017

    PEDFUSE

    FDA Adverse Event
    Malfunction ·SPINEFRONTIER, INC·Product code MNH·October 17, 2017