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

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    Revolution Spinal Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRECISION MONTAGE MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 24, 2020

    LINEAR? ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·August 20, 2025

    CAPILLARY'S IMMUNOTYPING (PN 2100)

    FDA 510(k)
    FDA Class 2 ·Immunology

    FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR MODEL KD-931

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD INSYTE¿ VIALON E IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·March 20, 2022

    OSCILL-SAW-ATTACHM F/532.001 532.010 532

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·October 6, 2014

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·May 30, 2013

    UNKNOWN DEPUY HEAD BALL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·June 23, 2011