BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    PMT Posterior Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ORS-100 FLUID WARMER DRAPE

    FDA Adverse Event
    Malfunction ·MICROTEK DOMINICANA, S.A.·Product code LHC·April 4, 2018

    MAGNETIC RESONANCE DIAGNOSTIC DEVICE

    FDA 510(k)
    FDA Class 2 ·Radiology

    INCU I

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AIR DERMATOME HANDPIECE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·June 5, 2013

    UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·July 22, 2011

    HEARTSTART SLA BATTERY

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DQA·September 19, 2014

    SPEED COMPRESSION IMPLANT KIT 25X20X20MM

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code JDR·October 1, 2019