BEUDAMED
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    LABELING CHANGE PCP (PHENCYCLIDINE) IN URINE

    FDA 510(k)
    FDA Unclassified ·Unknown

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867127302·GUIDE WIRE PLUNGER

    ULTRA CHEM CRESOLPHTHALEIN CALCIUM 65082

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Certus 140 2.45GHz Ablation System

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

    5.0MM, DRL BIT, CANNULATED, REUSABLE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HTW·May 26, 2026

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 2, 2014

    ECHELON*FLEX60 ARTICULATING

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·December 14, 2012

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 29, 2015