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

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    MANUAL RESUSCITATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756379199·HIP PACK

    RALCO

    FDA 510(k)
    FDA Class 2 ·Radiology

    STERILE BRIGHTWAY BRAND POWER-FREE, LATEX EXAMINATION GLOVES, WITH PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS) TESTED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ACUITY

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·January 11, 2013

    GENESIS IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROSTIMULATION·Product code LGW·November 23, 2010

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 2, 2014

    REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER Ø39/+3MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·July 22, 2022

    INSERTER-MEDIUM

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·June 18, 2019