BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    PERCUTANEOUS NEPHROSTOMY CATHETER

    FDA 510(k)
    FDA Unclassified ·Unknown

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0330080·Rocker, Hinged, Locking

    AIR SAFETY HEPA AND NON-HEPA FILTERS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BNX DELIVERY SYSTEM PRE-LOADED WITH 19, 22 AND 25 GAUGE NEEDLE, 19, 22 OR 25 GAUGE NEEDLES (INDIVIDUALLY STERILE-PACKED,

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

    ORTHOLOCK EX-PIN 3X110

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HAW·May 27, 2014

    UNKNOWN RIGHT ABGII HIP

    FDA Adverse Event
    Injury ·STRYKER IRELAND, LTD. OSTEONICS (ORTHOPAEDICS DIVI·Product code JDI·October 30, 2012

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 9, 2015

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015