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

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    CUFFED ENDOTRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·SHERIDAN CATHETER CORP.·Product code BTR·April 18, 1996

    SHERIDAN NASAL TUBE

    FDA Adverse Event
    Injury ·SHERIDAN CATHETER CORP.·Product code CAT·January 31, 1994

    SHERIDAN ET TUBE

    FDA Adverse Event
    Injury ·SHERIDAN CATHETER CORP.·Product code BSK·January 5, 1994

    ET TUBE, 7.0

    FDA Adverse Event
    Malfunction ·SHERIDAN CATHETER CORP.·March 17, 1994

    FLEXIBAND CUFFED ORAL RAE TRACHEAL TUBE WITH CUFF, 8.0

    FDA Adverse Event
    SHERIDAN CATHETER CORP.·Product code BTR·February 23, 1995

    SHERIDAN

    FDA Adverse Event
    Injury ·SHERIDAN CATHETER CORP.·Product code BSK·March 7, 1995

    OHIO ENDOTRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·SHERIDAN CATHETER CORP.·Product code BTR·October 10, 1994

    SHERIDAN

    FDA Adverse Event
    Injury ·SHERIDAN CATHETER CORP.·Product code BTR·May 23, 1997

    CF CUFFED TRACHEAL TUBE MURPHY EYE, 8.0

    FDA Adverse Event
    Injury ·SHERIDAN CATHETER CORP.·Product code BTR·April 28, 1995

    ENDOTRACHEAL TUBE

    FDA Adverse Event
    SHERIDAN CATHETER, CORP.·Product code BTR·October 10, 1995

    ENDOTRACHEAL TUBE, 3.5

    FDA Adverse Event
    Injury ·SHERIDAN CATHETER CORP.·Product code BTR·December 3, 1993

    ENDOTRACHEAL TUBE, 7.5

    FDA Adverse Event
    Injury ·SHERIDAN CATHETER CORP.·Product code BTR·September 1, 1994

    UNKNOWN

    FDA Adverse Event
    Death ·SHERIDAN CATHETER CORP.·Product code BTR·September 27, 1994

    SHERIDAN

    FDA Adverse Event
    Malfunction ·SHERIDAN CATHETER CORP.·Product code LNZ·July 13, 1992

    SHERIDAN

    FDA Adverse Event
    Injury ·SHERIDAN CATHETER CORP.·Product code BTR·August 15, 2001