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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    FUJINON

    FDA Adverse Event
    Malfunction ·FUJIFILM MEDICAL SYSTEMS U.S.A., INC.·Product code GDB·April 11, 2017

    FUJINON

    FDA Adverse Event
    Malfunction ·FUJINON, INC.·Product code EOQ·March 25, 2013

    FUJINON

    FDA Adverse Event
    Malfunction ·FUJINON, INC.·Product code EOQ·March 25, 2013

    FUJINON

    FDA Adverse Event
    Malfunction ·FUJINON INC.·Product code FDS·January 27, 2010

    FUJINON SINGLE-USE DOUBLE BALLOON OVERTUBE

    FDA Adverse Event
    Malfunction ·FUJINON, INC.·Product code GCJ·June 16, 2010

    EC 200LT

    FDA Adverse Event
    Malfunction ·FUJINON INC.·Product code KOG·April 12, 2000

    FUJINON HIGH-DEFINITION GASTROSCOPE

    FDA Adverse Event
    Malfunction ·FUJINON INC·Product code FDS·September 23, 2011

    FUJINON DUODENOSCOPE

    FDA Adverse Event
    Malfunction ·FUJINON, INC.·Product code FDT·October 22, 2008

    FUJINON HIGH-DEFINITION GASTROSCOPE

    FDA Adverse Event
    Malfunction ·FUJINON INC·Product code FDS·September 23, 2011

    FUJINON HIGH-DEFINITION GASTROSCOPE

    FDA Adverse Event
    Malfunction ·FUJINON INC·Product code FDS·September 23, 2011

    *

    FDA Adverse Event
    Malfunction ·FUJINON, INC.·Product code EOQ·November 23, 2007

    EC-250HL5

    FDA Adverse Event
    Malfunction ·FUJINON, INC.·Product code FDF·May 8, 2006

    FUJINON COLONOSCOPE

    FDA Adverse Event
    Malfunction ·FUJINON, INC.·Product code FDF·May 7, 2008

    FUJINON DBE SCOPE OVERTUBE

    FDA Adverse Event
    Malfunction ·FUJINON / FUJIFILM MEDICAL SYSTEMS USA, INC.·Product code FDA·May 15, 2018

    FUJINON

    FDA Adverse Event
    Malfunction ·FUJIFILM CORP.·Product code EOQ·July 1, 2011