BEUDAMED
    12 results · 41ms · 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 FDA Adverse Event ×

    TROCAR SETS FOR VITREORETINAL SURGERY

    FDA Adverse Event
    Injury ·STERIMEDIX LIMITED·Product code HMX·June 18, 2021

    SILKANN 23G CANNULA AND 21G PRE-HOLE NEEDLE

    FDA Adverse Event
    Injury ·STERIMEDIX LIMITED·Product code GEA·October 29, 2021

    HYDRODISSECTION CANNULA

    FDA Adverse Event
    Malfunction ·STERIMEDIX LIMITED·Product code HMX·October 19, 2020

    HYDRODISSECTION CANNULAE

    FDA Adverse Event
    Malfunction ·STERIMEDIX LIMITED·Product code HMX·September 19, 2023

    HYDRODISSECTION CANNULAE

    FDA Adverse Event
    Malfunction ·STERIMEDIX LIMITED·Product code HMX·September 19, 2023

    SILKANN FT CANNULA 27G X 37MM

    FDA Adverse Event
    Injury ·STERIMEDIX LIMITED·Product code GEA·October 29, 2021

    VISCOELASTIC CANNULA

    FDA Adverse Event
    Malfunction ·STERIMEDIX LIMITED·Product code HMX·October 2, 2023

    VISCOELASTIC CANNULA

    FDA Adverse Event
    Injury ·STERIMEDIX LIMITED·Product code HMX·February 14, 2024

    30G RYCROFT CANNULA

    FDA Adverse Event
    Malfunction ·Product code HMX·June 30, 2021

    27G X 7/8¿ VISCOELASTIC

    FDA Adverse Event
    Injury ·Product code HMX·July 13, 2021

    25G X 7/8¿ VISCOELASTIC

    FDA Adverse Event
    Injury ·Product code HMX·July 13, 2021

    BIOLON PRIME

    FDA Adverse Event
    Injury ·BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.·Product code MOZ·January 28, 2024