BEUDAMED
    7 results · 21ms · 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 ×

    Synapse 3D Blood Flow Analysis

    FDA 510(k)
    FDA Class 2 ·Radiology

    S-TEST LACTATE DEHYDROGENASE (LD), MODEL RC 0017

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    GLIDER PTCA BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SUBDURAL ELECTRODES, DEPTH ELECTRODES, AND ANCHOR BOLTS

    FDA Adverse Event
    Injury ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·June 14, 2019

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 27, 2011

    MATRIX2 ULTRASOFT 360 SR COIL

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIVISION·Product code HCG·October 7, 2008

    LARGE OSCILLATING SAW ATTACHMENT F/532.0

    FDA Adverse Event
    Malfunction ·SYNTHES (USA) BRANDYWINE·Product code HWE·June 26, 2013