BEUDAMED
    9 results · 34ms · Sources: EU EUDAMED, US FDA

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    2951239-1997-00002

    FDA Adverse Event
    Other ·Product code GCJ·July 23, 1997

    ZEPHIR ANTERIOR CERVICAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWQ·June 11, 2009

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 8, 2013

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·December 14, 2010

    STEALTHSTATION S7 SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·July 22, 2014

    TPRLC 133 MP TYPE1 PPS SO 17.0

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·September 10, 2024

    TPRLC 133 T1 PPS HO 13X146MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LZO·September 10, 2024

    TPRLC 133 T1 PPS HO 15X150MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LZO·September 10, 2024

    FREEDOM CONSTR. LINER +5 SZ 25

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWZ·May 13, 2022