BEUDAMED
    12 results · 75ms · Sources: EU EUDAMED, US FDA

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    NEEDLE DRIVER

    FDA Adverse Event
    Malfunction ·MITEK SURGICAL PRODUCTS, INC.·Product code GDF·February 8, 1995

    MITEK

    FDA Adverse Event
    Injury ·MITEK SURGICAL PRODUCTS, INC.·Product code KGS·June 27, 1997

    MITEK REAMERS 7MM, 8MM 9MM

    FDA Adverse Event
    Malfunction ·MITEK SURGICAL PRODUCTS, INC.·Product code HTO·October 29, 1996

    MITEK GII ANCHOR

    FDA Adverse Event
    Injury ·MITEK SURGICAL PRODUCTS, INC.·Product code KGS·October 29, 1996

    MITEK GII ANCHOR

    FDA Adverse Event
    Injury ·MITEK SURGICAL PRODUCTS, INC.·Product code KGS·December 2, 1996

    LIGATURE ANCHOR

    FDA Adverse Event
    Malfunction ·MITEK SURGICAL PRODUCTS, INC.·Product code KGS·May 9, 1995

    MITEK ANCHOR SYSTEM

    FDA Adverse Event
    Malfunction ·MITEK SURGICAL PRODUCTS, INC.·July 29, 1994

    MITEK ANCHOR SYSTEM

    FDA Adverse Event
    Malfunction ·MITEK SURGICAL PRODUCTS, INC.·Product code KGS·May 18, 1994

    MITEK

    FDA Adverse Event
    Injury ·MITEK SURGICAL PRODUCTS, INC.·Product code GEI·March 20, 1998

    Orthocord Suture, DePuy Mitek, a Johnson & Johnson Company; . DePuy Mitek, Inc. 325 Paramount Drive, Raynham, MA 02767 Sutures are intended for general soft tissue approximation and/or ligation.

    FDA Recall
    Terminated ·Ethicon, Inc. US·Product code NEW·February 2, 2009

    Orthocord Blue Braided Composite Suture, DePuy Mitek, A Johnson & Johnson Company, Meets USP and EP, except for diameter. DePuy Mitek, Inc. 325 Paramount Drive, Raynham, MA 02767 Sutures are intended for general soft tissue approximation and/or ligation.

    FDA Recall
    Terminated ·Ethicon, Inc. US·Product code NEW·February 2, 2009

    UNKNOWN MINI ANCHOR

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code HWC·September 30, 2019