BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    RESPITRACE 300SC

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209111404·STATION, BLEEDING CONTROL - INTERMEDIATE - NYLO...

    Powder Free Vinyl Patient Examination Gloves (Green)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SURETEK MEDICAL REPROCESSED ELECTROSURGICAL ELECTRODES

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

    HEDSTROEM M-ACCESS 21MM 015

    FDA Adverse Event
    Malfunction ·MAILLEFER INSTRUMENTS HOLDING SARL·Product code EKS·May 1, 2024

    OT ULTRA EASY METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014

    FLEXTEND

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·October 4, 2010

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·November 14, 2012

    DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE, E-MINIC AND ACCESSORIES. DATEX-OHMEDA S/5TM FM WITH L-FICU04 ANDL-FICUO4A SOFTWARE AND N-FCREC MODULE **(OUS only). E-miniC and accessories is indicated for monitoring C02 and respiration rate of all hospital patients.

    FDA Enforcement
    Class I ·Terminated·GE Healthcare, LLC·July 30, 2014