BEUDAMED
    8 results · 36ms · 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 ×

    TRAVERSE DENTAL CHAIR

    FDA Adverse Event
    ENGLE DENTAL SYSTEMS·Product code EIA·May 2, 2019

    STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·April 28, 2014

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·October 22, 2012

    4.0MM 90-S MAX SERFAS ENERGY SUCTION PROBE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY PUERTO RICO·Product code GEI·August 3, 2010

    IVAC PRIMARY PUMP SET

    FDA Adverse Event
    Malfunction ·ALARIS MEDICAL SYSTEMS, INC.·Product code FPA·March 26, 1998

    BD PLATE CAMPYLOBACTER SB 100MM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code JSJ·June 2, 2022

    BIOMONITOR 2-AF

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code MXD·July 1, 2024

    CARDIOMESSENGER II-S TLINE

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code OSR·July 1, 2024