BEUDAMED
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    ULTRASOUND GENERATOR MODLE 2270

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

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110973·STERILIZING CASE MEDIUM/SMALL

    Grasping forceps

    FDA UDI
    SOPRO-COMEG GmbH·04059082022666·

    MODEL FAMILY OF AEROLASE ND:YAG LASERS: FRIENDLYLIGHT ND: YAG LASERS, FRIENDLYLIGHT NEO, LIGHTPOD ND: YAG LASERS, LIGHTP

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    A1CNOW FOR PROFESSIONAL USE

    FDA 510(k)
    FDA Class 2 ·Hematology

    TFNA SCREW 110MM - STERILE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·December 17, 2018

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·December 10, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 8, 2014

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 17, 2012