BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    CDT CYTOTOXI TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867047501·LO-PRO SCRW TM,SS 3.5X 60MMCORT

    EXPANDED SPECTRUM PHOTO THERAPY DEVICE, MODEL ESPT-3X

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Luna 3D GEN2 Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LO-PRO SCRW TM,SS 3.5X 60MMCORT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWC·February 6, 2023

    PUMP IN STYLE ADVANCED BREASTPUMP STARTER

    FDA Adverse Event
    Injury ·MEDELA, INC.·Product code HGX·June 9, 2014

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·December 21, 2012

    EPIDURAL CATHETERIZATION KIT

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL·Product code CAZ·September 28, 2010

    XP-CR Tibial Tray - Interlok 67mm Item # 195271

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·September 18, 2019