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 ×

    CERAVITAL CERAMIC OSSICULAR REPL. PROS.

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ATLANTIS SR PLUS CORONARY IMAGING CATHETER, MODEL 35975

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CARE BACK PAIN RELIEF STIMULATOR; CARE BACK PAIN RELIEF STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 9, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 31, 2012

    CE INTERMATE LV 50, 24 PACK, 50126

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·August 23, 2010

    Synthes Periarticular Insertion Handle for 4.5mm LCP Proximal Tibia Plates and Periarticular Aiming Arm for 4.5mm LCP Proximal Tibia Plates

    FDA Enforcement
    Class II ·Terminated·Synthes (USA) Products LLC·October 14, 2015