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

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    System, Test, Carcinoembryonic Antigen

    FDA Pre-Market Approval
    FDA Class 2 ·ENZYMUN TEST{R} CEA

    Tissue Graft Of 6mm And Greater

    FDA Pre-Market Approval
    FDA Class 3 ·N.C.G.T. GRAFT

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·CUSTOMEYES 70L & 79L (LIDOFILCON A&B)

    DENPAX

    FDA 510(k)
    FDA Class 1 ·Dental

    Tissue Graft Of 6mm And Greater

    FDA Pre-Market Approval
    FDA Class 3 ·N.C.G.T. GRAFT

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·CUSTOMEYES 70L & 79L (LIDOFILCON A&B)

    Tissue Graft Of 6mm And Greater

    FDA Pre-Market Approval
    FDA Class 3 ·N.C.G.T. GRAFT

    Tissue Graft Of 6mm And Greater

    FDA Pre-Market Approval
    FDA Class 3 ·BIOPOLYMERIC(TM) VASCULAR GRAFT

    Tissue Graft Of 6mm And Greater

    FDA Pre-Market Approval
    FDA Class 3 ·N.C.G.T. GRAFT

    Tissue Graft Of 6mm And Greater

    FDA Pre-Market Approval
    FDA Class 3 ·N.C.G.T. GRAFT

    Tissue Graft Of 6mm And Greater

    FDA Pre-Market Approval
    FDA Class 3 ·N.C.G.T. GRAFT

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·CUSTOMEYES 70L & 79L (LIDOFILCON A&B)

    Tissue Graft Of 6mm And Greater

    FDA Pre-Market Approval
    FDA Class 3 ·BIOPOLYMERIC(TM) VASCULAR GRAFT

    Tissue Graft Of 6mm And Greater

    FDA Pre-Market Approval
    FDA Class 3 ·N.C.G.T. GRAFT

    Tissue Graft Of 6mm And Greater

    FDA Pre-Market Approval
    FDA Class 3 ·N.C.G.T. GRAFT

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 10, 2014

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 31, 2012

    VIKING M WIRELESS

    FDA Adverse Event
    Injury ·LIKO AB·Product code FSA·June 17, 2015

    CARPENTIER-EDWARDS PERIMOUNT MAGNA AND MAGNA EASE PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code DYE·October 4, 2013

    SEE H10

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DYE·August 29, 2014