BEUDAMED
    1,730 results · 18ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VIGOR MODEL 2880 SOFTWARE APPLICATION

    Programmer, Pacemaker

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 2901 PROGRAMMERR SYSTEM

    Fluid, Intraocular

    FDA Pre-Market Approval
    FDA Class 3 ·Perfluoron

    Programmer, Pacemaker

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 2901 PROGRAMMER

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·CENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·IntellaNav MiFi XP amd IntellaNav XP

    Ligaments And Tendons, Synthetic

    FDA Pre-Market Approval
    FDA Class 3 ·KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE

    Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)

    FDA Pre-Market Approval
    FDA Class 3 ·Light Adjustable Lens (LAL), Light Delivery Device (LDD) System

    Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)

    FDA Pre-Market Approval
    FDA Class 3 ·LIGHT ADJUSTABLE LENS (LAL) AND LIGHT DELIVERY DEVICE (LDD)

    Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)

    FDA Pre-Market Approval
    FDA Class 3 ·Light Adjustable Lens (LAL) and Light Delivery Device (LDD)