BEUDAMED
    8 results · 25ms · 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: Injury ×

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·April 22, 2013

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code KWA·April 15, 2011

    CAPIOX CUSTOM PACK

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code DTZ·June 10, 2023

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 7, 2023

    CAPIOX CUSTOM PACK

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 7, 2023

    CAPIOX CUSTOM PACK

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 7, 2023

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·January 25, 2023

    UNSPECIFIED BD INSYTE¿ AUTOGUARD¿ IV CATHETER

    FDA Adverse Event
    Injury ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·February 11, 2016