BEUDAMED
    8 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.

    ANGIOMED INTRODUCING SETS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SALTZMAN STETHOSCOPE HEAD

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    INFRAVIEW/INFRASION-TELETHERMOGRAPHIC SYSTEM

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·June 16, 2014

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 19, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 16, 2012

    HT X-DRIVE SCREW, Part # 91-2416, W.Lorenz Surgical. Screws for use in the stabilization and fixation of mandibular fractures and mandibular reconstructive surgical procedures.

    FDA Recall
    Terminated ·Biomet Microfixation, Inc.·Product code JEY·July 11, 2008

    TFN-ADVANCED Proximal Femoral Nailing System (TFNA); for treatment of fractures in orthopedics and trauma.

    FDA Enforcement
    Class II ·Terminated·Synthes, Inc.·May 20, 2015