BEUDAMED
    10 results · 22ms · Sources: EU EUDAMED, US FDA

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    Duet External Drainage and Monitoring System (EDMS)

    FDA 510(k)
    FDA Class 2 ·Neurology

    MITEK

    FDA UDI
    Medos International Sàrl·10886705029075·Sheath with 1 Rotating Stopcock compatible with...

    NA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295122623·REV INST STER TRAY SECOND

    3M STERI-VAC STERILIZER/AERATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NUVASIVE MAXCESS LIGHT GUIDE

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

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PML·February 26, 2026

    AUTOSUTURE ENDO STITCH 10MM

    FDA Adverse Event
    Malfunction ·COVIDIEN UNITED STATES SURGICAL CORPORATION·Product code MFJ·November 20, 2008

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·September 9, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code PML·November 13, 2025