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

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    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·CHIROFLEX MODELS 32 C10XX SILICONE POSTERIOR IOL

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·SILICONE INTRAOCULAR LENSES

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·CHIROFLEX(TM) ADD MODEL 32-C11XX SINGLE PIECE IOL

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·CHIROFLEX(TM) SINGLE PIECE SILICONE POST. CHAM.IOL

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·UV-ABSORBING SILICONE POSTERIOR CHAMBER INTRAOCULAR LENSES WITH PLATE HAPTICS

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·CHIROFLEX(TM) MODEL C10UB ULTRAVIOLET-ABSORBING SILICONE POSTERIOR CHAMBER INTRAOCULAR LENS

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·ULTRAVIOLET-ABSORBING SILICONE POSTERIOR CHAMBER INTRAOCULAR LENSES,MODEL C11UB

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL C11UB ULTRAVIOLET-ABSORBING SILICONE POSTERIOR CHAMBER INTRAOCULAR LENS

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·CHIROFLEX(TM)MODEL C10UB ULTRAVIOLET-ABSORBING SILICONE POSTERIOR CHAMBER INTRAOCULAR LENS

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·CHIROFLEX(TM) MODEL 32-C10XX SILICONE POS.CHA.IOL

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·CHIROFLEX(TM)MODEL C10UB ULTRAVIOLET-ABSORBING SILICONE POSTERIOR CHAMBER INTRAOCULAR LENS

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756978262·EXTREMITY PACK

    Equator Attachment H3mm

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118143406·Equator Attachment H3mm

    Plastic Cylinder with Hex Ti

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118141693·Plastic Cylinder with Hex Ti

    Plastic Cylinder with Hex Ti

    FDA UDI
    T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190011215·

    Agilis

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935108337·

    Bone Sonometer

    FDA Pre-Market Approval
    FDA Class 2 ·OSTEOSPACE

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·FLEXLENS (HEFILCON A) SOFT CONTACT LENSES

    ENTERRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LNQ·November 24, 2010

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES·Product code LZG·February 25, 2014