BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    Caduceus S

    FDA 510(k)
    FDA Class 2 ·Neurology

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776394004·Replacement Stylet (with needle) for 72-5220553

    MODIFICATION TO UNIVERSAL TOTAL WRIST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARM-TYPE FULLY AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, WRIST-TYPE FULLY AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ULTRASITE ADDITIV PRIMARY I.V.SET

    FDA Adverse Event
    Other ·B. BRAUN OF DOMINICAN REPUBLIC·Product code FPA·October 29, 2008

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·August 23, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013

    BD CATHENA¿ SAFETY IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·July 7, 2022

    BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal specimens Catalog Number: 444213

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Co.·April 21, 2021