BEUDAMED
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    LOGIQ P9; LOGIQ P7

    FDA 510(k)
    FDA Class 2 ·Radiology

    Sonic

    FDA UDI
    Sonic Innovations, Inc.·05711583029993·EXPRESSFIT 2017

    POLAROID CONTACTSPOD

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    COOLTOUCH MODEL CT3PZ, COOLTOUCH CT3 PLUS COOLBREEZE

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

    ULTRAXX NEPHROSTOMY BALLOON AND SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LJE·August 8, 2024

    6000CMS IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 6, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·July 28, 2011

    PRECISION

    FDA Adverse Event
    Malfunction ·BOSOTN SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·September 30, 2008