BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    MICROSTAAR INJECTOR MODELS MSI-TD & MSI-PD (MODIFICATION)

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    VENTRALIGHT

    FDA UDI
    Davol Inc.·00801741031632·Ventralight ST Mesh, 6" (15.2 cm), Circle

    L582 TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    NEUROLOGICAL SPONGE

    FDA 510(k)
    FDA Class 2 ·Neurology

    VENTRALIGHT ST MESH

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC. -1213643·Product code FTL·August 31, 2021

    PULSE-GENERATOR, PACEMAKER, EXTERNAL

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code DTE·February 11, 2013

    TOOL LGD 12CM 2.5MM MATCH LG

    FDA Adverse Event
    Malfunction ·MDT POWERED SURGICAL SOLUTIONS·Product code HBE·January 10, 2011

    INTERGARD KNITTED GRAFT

    FDA Adverse Event
    Injury ·INTERVASCULAR, SAS·Product code DSY·July 16, 2014

    VENTRALIGHT ST MESH

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC. -1213643·Product code FTL·May 8, 2026