BEUDAMED
    8 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.

    OHIO VOLUME INCENTIVE SPIROMETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ANSPACH DISSECTION TOOLS

    FDA 510(k)
    FDA Class 2 ·Neurology

    3M Filtek Universal Restorative

    FDA 510(k)
    FDA Class 2 ·Dental

    FLEXI-SEAL CONTROL FMS KIT US

    FDA Adverse Event
    Malfunction ·CONVATEC, INC.·Product code KNT·March 31, 2014

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·October 31, 2012

    FOLFUSOR SV 4ML/H

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·August 24, 2010

    1.55MM X 10MM FLUTED TWIST DRL

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBE·October 17, 2016

    1.55MM X 10MM FLUTED TWIST DRL

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBE·October 17, 2016