BEUDAMED
    1,092 results · 24ms · 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 Regulation: Us FDA ×

    AFFINITY NT BALANCE

    FDA Adverse Event
    Injury ·PERFUSION SYSTEMS·Product code DTZ·May 3, 2024

    AFFINITY NT BALANCE

    FDA Adverse Event
    Injury ·PERFUSION SYSTEMS·Product code DTZ·May 3, 2024

    EKG ELECTRODE

    FDA Adverse Event
    Malfunction ·GRAPHIC CONTROLS CORP.·Product code DRX·October 17, 1996

    ALLEGRETTO WAVE EYE-Q EXCIMER LASER

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·June 30, 2017

    DAILIES TOTAL 1 MULTIFOCAL

    FDA Adverse Event
    Injury ·CIBA VISION GMBH·Product code LPL·June 8, 2018

    OASYS

    FDA Adverse Event
    Other ·Product code LPL·March 27, 2009

    EASYPUMP

    FDA Adverse Event
    Injury ·B. BRAUN MELSUNGEN AG·Product code MEB·March 21, 2023

    EASYPUMP

    FDA Adverse Event
    Injury ·B. BRAUN MELSUNGEN AG·Product code MEB·March 21, 2023

    INTRALASE FS2

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·June 30, 2017

    EASYPUMP

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code MEB·May 23, 2023

    ACUVUE OASYS WITH HYDRACLEAR PLUS

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·June 23, 2009

    ACUVUE ADVANCE WITH HYDRACLEAR

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·June 23, 2009

    ACUVUE OASYS WITH HYDRACLEAR PLUS

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·June 23, 2009

    ACUVUE OASYS WITH HYDRACLEAR PLUS

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·June 23, 2009

    ACUVUE OASYS WITH HYDRACLEAR PLUS

    FDA Adverse Event
    Other ·VISTAKON, JOHNSON AND JOHNSON·Product code LPL·May 8, 2008

    INTRALASE FS2

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HNO·January 30, 2020

    BIOFINITY SPHERE (COMFILCON A)

    FDA Adverse Event
    Injury ·COOPERVISION MANUFACTURING, LTD.·Product code LPM·December 6, 2019

    HU-FRIEDY EXCAVATOR (SUSPECTED)

    FDA Adverse Event
    Injury ·HU-FRIEDY MFG CO., LLC·Product code EKC·September 2, 2015

    EXCAVATOR DOUBLE ENDED 13-14

    FDA Adverse Event
    Malfunction ·MAILLEFER INSTRUMENTS HOLDING SARL·Product code EKC·July 22, 2024

    EXCAVATOR DOUBLE ENDED USA 17

    FDA Adverse Event
    Malfunction ·MAILLEFER INSTRUMENTS HOLDING SARL·Product code EKC·December 22, 2025