BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    ACUSON P200 Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    Oticon

    FDA UDI
    Oticon A/S·05707131339720·SIYA 1, KIT 312 NFM 85 L C001

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111246579·BROPHY DRESSING FCP STR 1X2 8"

    WATERLASE C100, MODEL 7100104

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

    VOCARE MYHEALTH TABLET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COCHLEAR OSIA OSI300 IMPLANT

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code PFO·March 8, 2026

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 22, 2025

    TAPERED TOOL LEGEND, F2/8TA23

    FDA Adverse Event
    Malfunction ·MEDTRONIC POWERED SURGICAL SOLUTIONS·Product code HBB·October 1, 2008

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2013

    NATURAL KNEE II STEMMED TIBIAL BASEPLATE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·July 22, 2011