BEUDAMED
    12 results · 17ms · 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: Other ×

    EDI OROGASTRIC CATHETER

    FDA Adverse Event
    Other ·COVIDIEN·Product code KNT·May 29, 2014

    SERVO-I

    FDA Adverse Event
    Other ·MAQUET CRITICAL CARE AB·Product code CBK·June 3, 2013

    SERVO-I

    FDA Adverse Event
    Other ·MAQUET CRITICAL CARE AB·Product code CBK·October 26, 2012

    EDI CATHETER

    FDA Adverse Event
    Other ·MAQUET·Product code CBK·August 5, 2011

    SERVO-I

    FDA Adverse Event
    Other ·MAQUET CRITICAL CARE AB·Product code CBK·May 8, 2013

    CARESUITE ED PULSECHECK

    FDA Adverse Event
    Other ·PICIS INC.·Product code NSX·June 10, 2010

    ENOVATE MEDICAL MOBIUS POWER

    FDA Adverse Event
    Other ·ENOVATE MEDICAL·Product code FCO·December 15, 2016

    SARNS 9000 PERFUSION SYSTEM, 115 V

    FDA Adverse Event
    Other ·3M HEALTH CARE/ SARNS AND CDI PRODUCTS·Product code DTQ·January 12, 1998

    LYNAL

    FDA Adverse Event
    Other ·DENTSPLY CAULK·Product code EBI·September 24, 2003

    COE-SOFT

    FDA Adverse Event
    Other ·GC AMERICA, INC.·Product code EBI·August 28, 2024

    LYNAL

    FDA Adverse Event
    Other ·DENTSPLY CAULK·Product code EBI·April 2, 2004

    ORTHODONTIC ANCHOR SYSTEM

    FDA Adverse Event
    Other ·Product code EBI·June 10, 2008