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

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    SYNTHES LOCKING HAND PLATES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CONMED

    FDA UDI
    Conmed Corporation·10845854004838·WIRE PASS DRILL, LONG, 1 X 19 MM

    G-SPERM, MODEL 10032

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

    U.S. TECHNOLOGIES, INC. RETRACTABLE SAFETY SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 18, 2024

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 3, 2013

    UNKNOWN ZIMMER KNEE IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code JWH·August 20, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 27, 2011