BEUDAMED
    88 results · 39ms · Sources: EU EUDAMED, US FDA

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    VITAL-PORT

    FDA Adverse Event
    Malfunction ·VITAL-PORT VASCULAR ACCESS·Product code LJT·January 29, 1998

    MYOCARDIAL SUTURELESS PERMANENT PACING LEAD

    FDA Adverse Event
    Other ·DAIG CORP.·Product code DTB·January 7, 1998

    RESTORE 5X10 SELF-TAPPING IMPLANT WITH MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·November 4, 1998

    UNK

    FDA Adverse Event
    Injury ·UNK·Product code DZE·January 24, 1998

    RESTORE 3.3X15 SELF-TAPPING IMPLANT WITH MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 11, 1998

    RUSSELL-TAYLOR

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC. ORTHOPAEDICS DIV.·Product code HWC·October 22, 1998

    GENESIS TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW INC. ORTHOPAEDICS DIV.·Product code HSH·June 29, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 12, 1998

    BIOMET ARCOM PATELLA

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code HTG·March 24, 1999

    VENTAK PRX III IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS·Product code LWS·March 6, 1997

    AUTO SUTURE CHEMOSITE TWO-PIECE POLYURETHANE SYSTEM

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code LCJ·August 27, 1997

    LIFE PAK

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL CORP.·Product code LDD·July 30, 1997

    AUTO SUTURE ROTICULATOR 55-4.8

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAG·June 18, 1997

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·June 22, 1998

    PACER LEADS

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·February 26, 1998

    MEDTRONIC

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·January 19, 1998

    STAT DL 9.5 FR. 40 CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code DSP·February 20, 1998

    AUTO SUTURE MULTIFIRE ENDO HERNIA 4.8MM DISPOSABLE LOADING U

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL CORP.·Product code GCJ·December 22, 1997

    TITANIUM SOLID TIBIAL NAIL

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HSB·July 24, 1998

    SUSTAIN 3.3X13 HA SCREW IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·June 12, 1998