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

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    LUOFUCON® Collagen Particles (Collagen Wound Dressing)

    FDA 510(k)
    FDA Unclassified ·Unknown

    IBL C3D-CIC EIA TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    SUNTOUCH EYE SPEAR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    BD INSYTE AUTOGUARD BC SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·July 21, 2020

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·November 14, 2008

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·July 19, 2011

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 18, 2013

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·August 15, 2017

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·August 15, 2017

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·August 15, 2017

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·August 14, 2017

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·August 14, 2017

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·August 15, 2017

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·August 15, 2017

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·August 14, 2017

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·August 15, 2017

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·August 15, 2017

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·August 14, 2017

    Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089; CD1235-40/100029272, 100029282, 100029311, 100031039, 100059779; CD1235-40Q/100029273, 100029295, 100029312, 100030840; CD1241-40/100046351; CD1241-40Q/100046167; CD2231-40/100029274, 100030110, 100041922; CD2231-40Q/100029275, 100030089, 100041923; CD2233-40/100029147, 100029276, 100029313, 100031066, 100037043, 100048759, 100070007; CD2233-40Q/100029148, 100029263, 100029314, 100031067, 100037044, 100059770, 100070068; CD2235-40/100029149, 100029265, 100029283, 100031029, 100059837; CD2235-40Q/100029239, 100029258, 100029284, 100031030, 100066504; CD2241-40/100046148; CD2241-40Q/100046149; CD2299-40/100056952

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