BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    ALLERCOAT ALLERGEN DISCS

    FDA 510(k)
    FDA Class 2 ·Immunology

    CODMAN®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780521419·CODMAN® Peel-Away Catheter Introducer 14FR.

    CODMAN®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780537410·CODMAN® Peel-Away Catheter Introducer

    CODMAN

    FDA UDI
    Cerenovus, Inc.·20886704042744·CODMAN Peel-Away Catheter Introducer 14 FR.

    Fix2Lock(Biocomposite medial, lateral, Biocombi Self Punching)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IMAGINE REFLEX

    FDA 510(k)
    FDA Class 2 ·Dental

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·May 24, 2014

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Injury ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·November 5, 2012

    STERLING ES PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LIT·September 10, 2010

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018