BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    Spiro-VISTA

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BD VENFLON PRO SAFETY SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·June 9, 2020

    EKOS MICRO-INFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Apex Revision Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KINECTIV TECHNOLOGY NECK PROVISIONAL

    FDA Adverse Event
    Malfunction ·ZIMMER, INC·Product code LXH·December 5, 2008

    PEDI PACK, RADIOPAQUE GAUZE WITHIN

    FDA Adverse Event
    Other ·MEDLINE INDUSTRIES, INC.·Product code GDY·September 10, 2011

    LARGE MOD HEAD ADAPT 12/14 +5

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code JDI·July 29, 2013