BEUDAMED
    61 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    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

    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

    LIFE PAK

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

    AUTO SUTURE MULTIFIRE ENDO HERNIA 4.8MM DISPOSABLE LOADING U

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

    SUSTAIN 3.3X13 HA SCREW IMPLANT

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

    2027763

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS·Product code DQO·July 23, 1997

    VASOSEAL VHD

    FDA Adverse Event
    Injury ·COLLAGEN PRODUCTS DIV BIOPLEX CORP. A SUBSIDIARY OF DATASCOPE CORP.·Product code MGB·March 9, 1998

    ORBIS SIGMA VALVE

    FDA Adverse Event
    Injury ·ELEKTA IMPLANTS, SA·Product code JXG·July 25, 1997

    MEDTRONIC

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·January 28, 1998

    CRYOVALVE

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code MIE·October 9, 1998

    STAT DL 9.5 FR. 40 CC IAB

    FDA Adverse Event
    Injury ·DATASCOPE CORPORATION·Product code DSP·February 24, 1998

    GLIDEWIRE GUIDEWIRE

    FDA Adverse Event
    Injury ·MEDI-TECH TERUMO MEDICAL CORP·Product code DQX·October 16, 1997