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

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    BARRIER BONE WAX APPLICATOR

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    SeaSpine Spacer System - Hollywood™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981031299·17mm Hollywood Trial, Lordotic

    MENS-O-MATIC 3000

    FDA 510(k)
    FDA Class 2 ·Neurology

    RECON-2 FLOW CONTROLLER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 7, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014

    GPS PROCEDURAL STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 3, 2010

    Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage: Device is intended for patient positioning.

    FDA Enforcement
    Class II ·Terminated·Med Tec Inc·June 10, 2020