BEUDAMED
    12 results · 30ms · Sources: EU EUDAMED, US FDA

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    Pac-Dent Barrier Sleeve, Cover-It(TM) Barrier Film

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

    Nautilus Spinal System

    FDA UDI
    Life Spine, Inc.·00190837054939·Nautilus Deflection Beam Handle

    Trulink

    FDA UDI
    Statcorp Medical·10841522123436·BP CUFF,TL SOFT,1T,CHILD,13-20CM,5/BG

    PHILIPS DREAM STATION 2

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 19, 2024

    CALLOS IMPACT AND INJECT BONE VOID FILLER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NEXFIN MODEL 2

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PENUMBRA SYSTEM MAX ASPIRATION TUBING

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·June 24, 2015

    20 G X .32 MM BD VENFLON¿ PRO SAFETY PERIPHERAL SAFETY IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·October 17, 2017

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

    ACUITY

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code OJX·July 6, 2011

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008

    Medical Linear Accelerator

    FDA Enforcement
    Class II ·Terminated·Elekta, Inc.·September 14, 2016