BEUDAMED
    63 results · 27ms · Sources: EU EUDAMED, US FDA

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    Lens, Contact (Rigid Gas Permeable), Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·MENICON SF-P RGP (MELAFOCON A) CONTACT LENS

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·MENICON SF-P (MELAFOCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·MENICON SUPER EX CONTACT LENS

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·MENICON SF-P (MELAFOCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·MENICON SUPER EX CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·MENICON SF-P RGP (MELAFOCON A) CONTACT LENS

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·MENICON SF-P (MELAFOCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·MENICON SF-P RGP (MELAFOCON A) CONTACT LENS

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·MENICON SF-P (TM)

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·MENICON SF-P RGP (MELAFOCON A) CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·MENICON SF-P RGP (MELAFOCON A) CONTACT LENS

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·MENICON SF-P (TISILFOCON A) RIGID GAS PERMEABLE CONTACT LENS

    Pro Advantage

    FDA UDI
    NATIONAL DISTRIBUTION & CONTRACTING, INC.·M220P8500982·Pro Advantage Electrode Foam

    VAN-TEC AUTO BIOPSY NEEDLE

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

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    SILICONE ULTRAVIOLET ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

    Fluid, Hysteroscopy

    FDA Pre-Market Approval
    FDA Class 3 ·DEXTRAN HM 32%

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·META-MV,PACING SYSTEM

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 8, 2006

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    FDA Adverse Event
    Malfunction ·STAAR SURGICAL·Product code HQL·June 15, 2006