BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ARX-LINK CROSS CONNECTOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 20, 2021

    EFILM WORKSTATION WITH MODULES

    FDA 510(k)
    FDA Class 2 ·Radiology

    NARKOMAT, MODEL 2000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SPRINT QUATTRO

    FDA Adverse Event
    Death ·MPRI·Product code LWS·April 22, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEM INC.·Product code JAA·July 10, 2008

    ACCU-CHEK RAPID D

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code FPA·April 20, 2011