BEUDAMED
    10,000 results · 25ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (SENOFILCON A) CONTACT LENSES/CLEAR & VISIBILITY TINTED WITH UV BLOCKER

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·Vistakon (senofilcon A) Brand Contact Lenses

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (senofilcon A) Brand Contact Lenses

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (Senofilcon A) Brand Contact Lenses

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (SENOFILCON A) BRAND CONTACT LENSES

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (senofilcon A) Brand Contact Lenses

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (senofilcon A) Brand Contact Lenses

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (SENOFILCON A) CONTACT LENS, CLEAR AND VISIBILITY TINTED WITH UV BLOCKER

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (SENOFILCON A) CONTACT LENS

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON SENOFILCON A BRAND CONTACT LENSES

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (SENOFILCON A) CONTACT LENSES

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·VISTAKON (senofilcon A) Brand Contact Lenses

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·TREO® Abdominal Stent-Graft System

    MEDILAS 2

    FDA 510(k)
    FDA Class 3 ·Unknown

    OPTIMA MPT MODEL 5281E AND MODEL 5282E

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    OPTIMA MPT SERIES III PACEMAKER, UNIPOLAR/BIPOLAR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    MODIFIED J-STIFFENER WIRE MATERIAL IN LEAD LINES

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    STERILIZATION

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    MODIFIED ANCOR & HI-FLEX UNIPOLAR ACTIVE FIX. LEAD

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    LIFE+CEL OR LIFECEL BATTERY PACK, MODEL 5L500

    FDA 510(k)
    FDA Class 3 ·Cardiovascular