BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    X-REPAIRSL

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

    JOURNEY CR KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SSA-770A, APLIO VERSION 5.5

    FDA 510(k)
    FDA Class 2 ·Radiology

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWP·November 7, 2019

    ADVIA CENTAUR XPT

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·July 19, 2016

    GORE® SEAMGUARD® BIOABSORBABLE STAPLE LINE REINFORCEMENT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code FTM·October 28, 2021

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 1, 2011

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·October 4, 2014