BEUDAMED
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    U BY KOTEX CLICK* UNSCENTED TAMPONS, MODEL ABSORBENCY: REGULAR, SUPER AND SUPER PLUS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    HERNIATOME

    FDA UDI
    ADRIA SRL·08033737119983·Percutaneous Discectomy Device

    EBI DYNAFIX VS OSTEOTOMY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LATEX POWDERED PATIENT EXAMINATION GLOVE, 200 MICROGRAMS OR LESS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PANORAMA WITH TELEMETRY

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·April 30, 2013

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·September 16, 2014

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 17, 2011

    Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749

    FDA Recall
    Terminated ·ADRIA SRL Via Modena 46 Societa Unipersonale San Giovanni In Persiceto Italy·Product code HRX·May 17, 2021

    Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749

    FDA Enforcement
    Class II ·Terminated·ADRIA SRL·October 27, 2021