BEUDAMED
    228 results · 22ms · Sources: EU EUDAMED, US FDA

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    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

    ELLIPSE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COLLAGEN TEST IMPLANT

    FDA Adverse Event
    Injury ·COLLAGEN CORP·Product code LMH·April 14, 1998

    TRIUMPH-1

    FDA Adverse Event
    Injury ·HORIZON MEDICAL PROD·Product code LJT·October 28, 1997

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code DSP·November 25, 1997

    RECTAL THERMOMETER

    FDA Adverse Event
    Injury ·FAICHNEY MEDICAL CO.·Product code FLK·July 15, 1997

    PERCOR STAT DL 9.5 FR 40 CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 24, 1997

    RESTORE 4X13 SELF-TAP

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

    RESTORE 3.4X13 TPS CYLIND

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·March 2, 1998

    RESTORE 3.3X8 SELF-TAP

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

    SUSTAIN 3.3X15 HA CYLINDER IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 17, 1998

    RESTORE 6X8 SELF-TAPPING IMPLANT WITH MOUNT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·August 19, 1998

    RESTORE 4X10 SELF-TAPPING IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·August 19, 1998

    RESTORE 3.75X15 SELF-TAPPING IMPLANT WITH MOUNT

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

    SUSTAIN 3.3X10 HA CYLINDER IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·September 24, 1998

    RESTORE 3.4X10 TPS CYLIND

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·April 7, 1998

    SERIES TEN THOUSAND OCUTOME

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·July 22, 1997

    SUSTAIN 3.3X13 HA CYLINDER IMPLANT

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·August 19, 1998

    VISCOAT

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