BEUDAMED
    10 results · 33ms · Sources: EU EUDAMED, US FDA

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    H/S CATHETER SET FOR HYSTEROSALPINGOGRAPHY

    FDA Adverse Event
    Malfunction ·ACKRAD LABORATORIES·Product code HDN·June 30, 2000

    INCUBATOR/FLUID WARMER

    FDA Adverse Event
    Other ·ACKRAD LABORATORIES·Product code LGZ·February 22, 1996

    TRAKE-KIT

    FDA Adverse Event
    Death ·ACKRAD LABORATORIES, INC.·Product code CBH·June 24, 1996

    NEO-FIT

    FDA Adverse Event
    Malfunction ·ACKRAD LABORATORIES INC.·Product code CBH·June 29, 2000

    H/S CATHETER SET

    FDA Adverse Event
    Injury ·ACKRAD LABORATORIES, INC.·Product code MOV·June 5, 1997

    NEO-FIT NEONATAL ENDOTRACHEAL TUBE GRIP

    FDA Adverse Event
    Injury ·ACKRAD LABORATORIES, INC.·Product code CBH·May 27, 2003

    INCA

    FDA Adverse Event
    Injury ·ACKRAD LABORATORIES, INC.·Product code BYE·August 10, 1999

    NEO-FIT

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL (FORMERLY ACKRAD LABORATORIES, INC.)·Product code CBH·October 8, 2003

    FRIGITRONICS CCS-200

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, (FORMERLY: ACKRAD LABORATORIES, INC.)·Product code GEH·April 20, 2006

    H/S CATHETER SET

    FDA Adverse Event
    Injury ·ACKARD LABORATORIES, INC.·Product code LKF·August 8, 1995