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

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    8 mm SureForm 30 Curved-Tip Stapler, 8 mm SureForm 30 Stapler, SureForm 30 Reloads

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ZYPLAST COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·COLLAGEN CORP.·Product code LMH·October 10, 1997

    IMAGE1 GI CCU MODEL 22203020-114

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MODULAR VALVE HANDLES FOR ADAPTABLE TUBES, MODEL 1298-XX-XX, 1295-XX-XX

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    DEPUY CAPTURED HIP SCREW SIDE PLATE

    FDA Adverse Event
    Malfunction ·DEPUY ACE MEDICAL CO.·Product code KTT·August 4, 1997

    CHORUS

    FDA Adverse Event
    Other ·ELA MEDICAL, INC.·Product code DXY·April 29, 1997

    RESTORE 4X7 SELF-TAP

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·January 6, 1998

    RESTORE 3.3X8 SELF-TAP +

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·May 6, 1998

    HIP SCREW SYSTEM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC/ORTHOPAEDICS DIV.·Product code HSB·November 10, 1998

    RESTORE 3.75X10 SELF-TAP +

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·May 6, 1998

    RESTORE 4X13 TPS CYLINDER

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·January 21, 1998

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·October 31, 1997

    SILTEX SALINE MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FWM·July 10, 1998

    SERIES TEN THOUSAND OCUTOME

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·October 31, 1997

    SDI THREADED FUSION CAGE

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL CORP.·Product code MAX·August 15, 1997

    *

    FDA Adverse Event
    Malfunction ·ELA MEDICAL, S.A.·Product code DTB·August 18, 1997

    SMOOTH SALINE MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FWM·May 18, 1998

    UNK

    FDA Adverse Event
    Other ·SAFESKIN CORP.·Product code LYY·June 17, 1999

    CERVICAL SPINE LOCKING PLATE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code JDN·July 7, 1998

    SPECTRUM CONTOUR POST-OPERATIVELY ADJUSTABLE MAMMARY PROSTHE

    FDA Adverse Event
    Injury ·MENTOR·Product code FWM·August 31, 1998