BEUDAMED
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    IFSA STERILE SILK BRAIDED NONABSOR SURG SUTURES

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

    PUR® Implant Driver - Latch

    FDA UDI
    STERNGOLD DENTAL LLC·00841549118104·Used to turn the implant as it is screwed into ...

    MRT 50A CRANIO-CERVICAL COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    INTHERM TEMPORARY OCCLUSION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NCB, FEMUR PLATE, RIGHT, 9 HOLES, 246 MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HRS·October 7, 2019

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·January 9, 2013

    COLLEAGUE CXE VOLUMETRICINFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 22, 2010

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014

    Natus Quantum System with NeuroWorks Software. Catalog /Part Numbers: 013926. The Natus Quantum Amplifier is intended to be used as an electroencephalograph: to acquire, display, store and archive electrophysiological signals. The amplifier should be used in conjunction with Natus NeuroWorks /SleepWorks software to acquire scalp and intracranial electroencephalographic (EEG) signals as well as polysomnographic (PSG) signals.

    FDA Recall
    Terminated ·Natus Neurology DBA Excel Tech., Ltd. (XLTEK)·Product code GWQ·November 11, 2015