BEUDAMED
    7 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 ×

    SCINITREX (GREEN POWDERED NITRILE EXAMINATION GLOVES)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NON-BR2000 LARGE BONE BLADES

    FDA UDI
    Peter Brasseler Holdings, LLC·00887919095194·KM519-21

    THE EDGE DETECTOR, MODEL 1118

    FDA 510(k)
    FDA Class 2 ·Radiology

    STERISPINE PS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LIFE PULSE

    FDA Adverse Event
    Malfunction ·BUNNELL, INC.·Product code LSZ·June 27, 2014

    ELECTRODE, PACEMAKER, PERMANENT

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    CONFIENT

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 7, 2011