BEUDAMED
    11 results · 56ms · 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.

    DEROYAL

    FDA Adverse Event
    Injury ·ORTHO AND SURGICAL PRODUCTS ENTERPRISES S.A.·Product code FMQ·October 28, 2019

    CITADEL PATIENT CARE SYSTEM

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH POLSKA SP Z O.O·Product code FNL·May 23, 2018

    IMPELLA

    FDA Adverse Event
    Malfunction ·ABIOMED, INC. - 1220648·Product code OZD·February 27, 2026

    BARDEX® LUBRI-SIL® ALL-SILICONE TEMP SENSING FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·April 23, 2020

    CONCERTO, BASIC & SHOWER TROLLEY

    FDA Adverse Event
    Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·March 22, 2010

    PIPELINE FLEX

    FDA Adverse Event
    Malfunction ·COVIDIEN (IRVINE)·Product code OUT·December 17, 2018

    PIPELINE FLEX W/SHIELD TECHNOLOGY

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA·Product code OUT·November 29, 2018

    PIPELINE FLEX

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. D/B/A EV3 NEUROVASCULAR·Product code OUT·November 29, 2018

    PIPELINE FLEX

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA·Product code OUT·December 12, 2018

    PIPELINE FLEX

    FDA Adverse Event
    Malfunction ·COVIDIEN (IRVINE)·Product code OUT·November 15, 2018

    PIPELINE FLEX

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA·Product code OUT·January 7, 2019