BEUDAMED
    10 results · 29ms · 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.

    MODIFICATION TO NXSTAGE SYSTEM ONE

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

    MACROPOREMX MANDIBULAR FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    BECKMAN COULTER DNASE B CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·March 23, 2022

    CADD MEDICATION CASSETTE

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·July 14, 2022

    CADD

    FDA Adverse Event
    Malfunction ·NULL·Product code FPA·August 17, 2021

    CADD MEDICATION CASSETTES

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·June 6, 2022

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 8, 2013

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·March 22, 2011

    HEARTSTREAM XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 8, 2008