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

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    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL P-11 MODIFIED J-LOOP POSTERIOR CHAMBER IOL

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·TIER A & B INTRAOCULAR LENSES

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867048652·SIZING TAMPS, 6MM-8MM

    Changer, Tube, Endotracheal

    FDA Pre-Market Approval
    FDA Class 2 ·ENDOTRACHEAL TUBE CHANGER

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·DELTA PACEMAKER SYS; VIGOR DDD MODEL 950

    IMPLANTIUM

    FDA Adverse Event
    Injury ·DENTIUM USA·Product code DZE·October 28, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·February 7, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 28, 2012

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 446 & 447 VISTA T PU.GEN. MODEL 2046 SOF.MOD

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 446 & 447 VISTA T,MODEL 940 & 941 VISTA DDD

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VISTA DDD MODEL 942 & 944 AND SOFTWARE MODULE MODEL 2052

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 446 & 447 VISTA T PU.GEN. MODEL 2046 SOF.MOD

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 925, 2040, 2041, 6564

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·DELTA PACEMAKER SYSTEM

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VIGOR DDD PACEMAKER SYSTEM

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 6577 STERILIZABLE TELEMETRY WAND

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 446 & 447 VISTA T PU.GEN. MODEL 2046 SOF.MOD

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 925, 2040, 2041, 6564

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·DELTA(R) PACEMAKER SYSTEM (VIGOR SSI AND DDD MODELS ONLY)

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·DELTA PACEMAKER SYSTRM; VIGOR DDD MODEL 950 (MASTER)