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

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    SYNFIX Evolution Secured Spacer System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Oticon

    FDA UDI
    Oticon A/S·05707131280992·NERA2 PRO, MINIBTE 312 WL 85 CBE

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100202·NEVYAS DRAPE SPECULUM OPEN WIRE

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100516·THORLAKSON EYE SPECULUM

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171027676·PESSARY, CUBE #2, W/DRAINS, 33mm

    EASYLYTE NA/K/CL/LI ANALYZER, MODEL 2020

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CANDELA FAMILY OF PULSE DYE LASER SYSTEMS

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

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 6, 2013

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 14, 2015