BEUDAMED
    254 results · 24ms · Sources: EU EUDAMED, US FDA

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    Mako Total Hip Application, Mako Total Knee Application

    FDA 510(k)
    FDA Class 2 ·Neurology

    Bernafon

    FDA UDI
    Bernafon AG·05711584086728·ZR3, KIT 312 2.4G NFM 90 R BE ZERENA 3

    KAIYANG ALUMINUM WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYSTEM-HIP

    FDA 510(k)
    FDA Class 2 ·Neurology

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·October 9, 1998

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·October 19, 1998

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·December 15, 1997

    STAT DL 9.5 FR 40 CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·April 1, 1998

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·March 9, 1998

    STAT DL 9.5 FR. 40 CC. IAB

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

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·April 1, 1998

    HOMECHOICE AUTOMATED PD SYSTEM 115 VOLT

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP·Product code FKX·April 17, 1998

    RESTORE 5X10 SELF-TAP+

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

    RESTORE 5X10 SELF-TAPPING IMPLANT WITH MOUNT

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

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    FDA Adverse Event
    Malfunction ·MCGHAN MEDICAL CORP.·Product code FWM·April 1, 1998

    9500 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·November 18, 1998

    RESTORE 4X15 SELF-TAP

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

    RESTORE 3.75X13 SELF-TAPPING IMPLANT WITH MOUNT

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

    RESTORE 4X13 TPS CYLINDER IMPLANT

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

    RESTORE 3.3X10 SELF-TAP +

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