BEUDAMED
    8 results · 22ms · 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 ×

    M300 & M400

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ArgenPMMA Multi98x30-B3

    FDA UDI
    ARGEN CORPORATION, THE·D818123290·Crown And Bridge, Temporary, Resin

    EDLEN IMAGING - GEMINI DUSB

    FDA 510(k)
    FDA Class 2 ·Dental

    STERRAD 50 & STERRAD 100S STERILIZERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·May 21, 2013

    UNI-KNEE MOD. TIBIAL BEAR INS.

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code HSX·September 26, 2014

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 14, 2011

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 20, 2025