BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PREMICATH PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·May 20, 2015

    PREMICATH PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·May 22, 2015

    PREMICATH

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·April 20, 2015

    PREMICATH

    FDA Adverse Event
    VYGON GMBH·Product code LJS·April 20, 2015

    PREMICATH PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·June 3, 2015

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·January 9, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2014

    ASR ACETABULAR CUPS 48

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 5, 2011

    ORTHOPEDIC SALVAGE SYSTEM MOD ARTHRO 0 DEG LCK COLLAR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSB·June 12, 2024

    23GA ILLUMINATED DIRECTIONAL LASER PROBE

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQB·March 19, 2020

    25GA ILLUMINATED DIRECTIONAL LASER PROBE

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQB·March 19, 2020