BEUDAMED
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    Vericor Support Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRIAL HEAD FOR BROACH ESOP HA D.32 +3,5

    FDA UDI
    FOURNITURES HOSPITALIERES INDUSTRIE·03661489226793·

    BD VACUTAINER® BUFFERED SODIUM CITRATE BLOOD COLLECTION TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·November 29, 2023

    Optional Screen Display for HeartSee Cardiac P.E.T. Processing Software - HeartSee version 3

    FDA 510(k)
    FDA Class 2 ·Radiology

    RAPHAEL

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    1688 AIM 4K CAMERA HEAD WITH INTEGRATED COUPLER - INTERNATIONAL KIT

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·September 13, 2024

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 25, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·November 4, 2014

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 12, 2013

    SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini Implantable Fusion Stimulators are indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels

    FDA Enforcement
    Class I ·Terminated·Zimmer Biomet, Inc.·November 7, 2018