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

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    Lenses, Soft Contact, Daily Wear

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

    Lenses, Soft Contact, Extended Wear

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

    Lenses, Soft Contact, Extended Wear

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

    Pro Advantage

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

    Tissue Graft Of 6mm And Greater

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

    DU PONT TOBRAMYCIN ASSAY REAGENTS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    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 ·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

    Lens, Contact (Polymethylmethacrylate)

    FDA Pre-Market Approval
    FDA Unclassified ·THE BOSTON LENS II ALGES(R) BIFOCAL CONTACT LENS

    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

    CORAIL2 NON COL HO SIZE 12

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS-3003895575·Product code KWA·June 4, 2014

    ALPHA INSERT ME NEUTRAL HH/28

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSH·November 26, 2012

    SM104 M-SERIES W/5TH WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER CORP, MEDICAL DIVISION·Product code FPO·September 27, 2010

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 9, 2016