BEUDAMED
    13 results · 28ms · 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.

    SCHUSTER DISPOSABLE BALLOON PROBE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CLICK'X MONOAXIAL SCREWS AND HOOKS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FILTRYZER HOLLOW FIBER ARTIF. KIDNEY

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BD ALARIS¿ SMARTSITE¿ GRAVITY SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·February 9, 2023

    MODEL NOT SPECIFIED

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·December 10, 2010

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·January 28, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 14, 2014

    BD GEM V/NV 20D 0.2 FLTR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·July 28, 2022

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWP·May 13, 2016

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWP·May 13, 2016

    GEM V/NV NTG 20DP 20PK

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 10, 2020

    BD ALARIS¿ SMARTSITE¿ GRAVITY SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·January 20, 2023

    XiO Radiation Treatment Planning System, XiO versions equal to or greater than 2.4.0 and less than 4.63.0 The XiO RTP System is used to create treatment plans for any cancer patient for whom external beam radiation therapy or brachytherapy has been prescribed.

    FDA Recall
    Terminated ·Computerized Medical Systems Inc·Product code MUJ·June 9, 2011