BEUDAMED
    14 results · 71ms · Sources: EU EUDAMED, US FDA

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    SITE MICROSURGICAL SYSTEMS, INC.

    FDA Adverse Event
    Injury ·SITE MICROSURGICAL SYSTEMS, INC.·Product code HQC·August 31, 1994

    VICRYL POLYGLACTIN 910 MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·December 21, 2021

    SITE MICROSURGICAL UNIT

    FDA Adverse Event
    Malfunction ·SITE MICROSURGICAL SYSTEMS, INC.·Product code HQC·July 5, 1996

    SITE MICROSURGICAL UNIT

    FDA Adverse Event
    Malfunction ·SITE MICROSURGICAL SYSTEMS, INC.·Product code HQC·July 5, 1996

    AUTOMATIC ASPIRATOR/IRRIGATOR

    FDA Adverse Event
    Injury ·SITE MICROSURGICAL SYSTEMS, INC.·Product code HQC·March 28, 1994

    TXR

    FDA Adverse Event
    Injury ·SITE-MICROSURGICAL SYSTEMS, INC.·Product code HQC·May 29, 1992

    TXR PHACOEMULSIFICATION MACHINE

    FDA Adverse Event
    Malfunction ·SITE MICROSURGICAL SYSTEMS, INC.·Product code HQC·September 20, 1994

    PHARCOEMULSIFICATION CATARACT SYSTEM

    FDA Adverse Event
    SITE MICROSURGICAL SYSTEMS, INC.·Product code HQC·July 29, 1994

    SAME

    FDA Adverse Event
    Malfunction ·SITE MICROSURGICAL SYSTEMS, INC.·Product code KBO·July 4, 1992

    MILLENIUM MICROSURGICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB SURGICAL, INC·Product code HQE·February 9, 2007

    SITE TXR MICROSURGICAL SYSTEM

    FDA Adverse Event
    Injury ·SITE MICROSURGICAL SYSTEM, INC.·Product code GZX·July 9, 1992

    SITE MICROSURGICAL UNIT

    FDA Adverse Event
    Malfunction ·SITE MICROSURGICAL SYSTEMS INC, DIV. OF CHIRON VISION CORP.·Product code HQC·June 30, 1996

    FlowCOUPLER. An implantable device that is used to detect blood flow in vessels. Used in the end-to-end anastomosis of veins and arteries normally encountered in microsurgical and vascular reconstructive procedures. The FlowCOUPLER System is intended to detect blood flow and confirm vessel patency intra-operatively and post-operatively at the anastomotic site. Baxter Healthcare.

    FDA Recall
    Terminated ·Baxter Healthcare Corporation·Product code DPW·July 11, 2014

    MDSS GmbH

    Authorized representative
    🇩🇪 Germany·388 Manufacturers·16562 Devices