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

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    Stimulator, Salivary System

    FDA Pre-Market Approval
    FDA Class 2 ·SALITRON SYSTEM

    Philips Brilliance IQon Spectral CT, Computed Tomography X-Ray System; Model # 728332; UDI # (01)00884838059542(21)860067

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·May 13, 2020

    MICROSCOPE COLUMN DRAPE

    FDA 510(k)

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH TM IMPLANTABLE PACEMAKER PULSE

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH(R)II MODELS 262-16

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH & INTERTACH II PULSE GENERATORS

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MAESTRO SERIES 500 P.G.& MODEL 1006 PACEMAKER PROG

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·IMPLANTABLE PACEMAKER LEADS

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH(R)II MODELS 262-16

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH(R)II MODELS 262-16

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH(R)II MODELS 262-16/262-16R DISCON.TEST

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH(R)II MODELS 262-16

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH & INTERTACH II PULSE GENERATORS

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH(R)II MODELS 262-16

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MAESTRO(R) RELEASE III SOFTWARE 5OO SERIES

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH II MODELS 262-16

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH(R)II MODELS 262-16

    Pulse-Generator, Single Chamber, Single

    FDA Pre-Market Approval
    FDA Class 3 ·INTERTACH