BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Aequalis PerFORM+ Shoulder System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sterile ACIF PEEK

    FDA UDI
    Tyber Medical, LLC·M6958101609750·ACIF o 16mm x 9mm x 7.5 deg PEEK Curved

    IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2

    FDA 510(k)
    FDA Class 2 ·Neurology

    NITRIL EXAM GLOVE, PRE-POWERED COLOR WHITE, NITRILE EXAM GLOVE, PRE-POWDERED, COLOR BLUE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 23, 2025

    OT ULTRASMART METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code LZS·June 16, 2011

    CAPSUREFIX

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVN·October 10, 2014