BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    ALLIS TISSUE FORCEPS, 4X5 TEETH, 6+SS 410 OR 420

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209113590·

    IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    JOURNEY II XR Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014

    PFC SIGMA CRVD INSERT SZ3 10MM

    FDA Adverse Event
    Injury ·DEPUY IRELAND·Product code JWH·November 30, 2012

    VITALITY 2

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 4, 2010

    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