BEUDAMED
    7 results · 25ms · 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.

    DR-2C

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    B-NEOCEPT 30

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    WALL GRAB BARS 98130-98136

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    UNK VENTRICLEAR II CATHETER

    FDA Adverse Event
    Other ·MEDTRONIC NEUROSURGERY·Product code JXG·May 20, 2014

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·November 12, 2012

    COROMETRICS QWIKCONNECT PLUS SPIRAL ELECTRODE

    FDA Adverse Event
    Injury ·GE HEALTH·Product code HGP·September 23, 2010

    BIOMET StageOne Knee Tibial Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 433165.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020