BEUDAMED
    7 results · 19ms · 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.

    REUSABLE MOIST HEAT PACK

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Freestyle Flex

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ARK LEVETIRACETAM ASSAY, ARK LEVETIRACETAM CALIBRATOR AND ARK LEVETIRACETAM CONTROL, MODELS 5024-0001-00, 5024-0002-00

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    INVISION-PLUS

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, LLC·Product code FPA·July 7, 2022

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 6, 2014

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·August 10, 2010