BEUDAMED
    8 results · 19ms · 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 Regulation: Us FDA ×

    HYDROCISION DEBDRIDEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VINYL POWDER FREE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CANDIDA IMMUNODIFFUSION KIT #CA1001

    FDA 510(k)
    FDA Class 2 ·Microbiology

    LEVEL 1 HOTLINE LOW FLOW SYSTEMS

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LGZ·January 23, 2024

    LEVEL 1 HOTLINE LOW FLOW SYSTEMS

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LGZ·January 23, 2024

    OT ULTRAMINI METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 6, 2013

    CONSULTA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·February 15, 2011

    SECURA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 8, 2014