BEUDAMED
    7 results · 20ms · 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 ×

    BD Nexiva and BD Nexiva Diffusics Closed IV Catheter Systems

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD¿ NEXIVA SINGLE PORT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 21, 2019

    U2 ACETABULAR CUP, PLASMA SPRAY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PIONEER PLUS CATHETER, MODEL PLUS 120

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    DXTEND METAGLENE

    FDA Adverse Event
    Malfunction ·3003895575 DEPUY FRANCE·Product code HSD·June 11, 2013

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·July 14, 2011