BEUDAMED
    8 results · 21ms · 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 ×

    NEURON MAX 6F 088 LONG SHEATH

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·February 10, 2016

    NEURON MAX 6F 088 LONG SHEATH

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·February 10, 2016

    EXODONTIA ELEVATOR #46R SERRATED

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·March 29, 2016

    HEARTMATE II SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·January 26, 2011

    EXODONTIA ELEVATOR #46R SERRATED

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·March 29, 2016

    EXODONTIA ELEVATOR #46R SERRATED

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code EMJ·March 29, 2016

    ANCHOR BOLTS

    FDA Adverse Event
    Malfunction ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·May 17, 2019

    MI-750

    FDA Adverse Event
    Malfunction ·MEDICAL ILLUMINATION INTRNATION INC.·Product code FSY·January 17, 2023