BEUDAMED
    9 results · 18ms · 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.

    LB-2000 CRANIAL ELECTROTHERAPY STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756363181·CATARACT PACK

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0106160·Trial, 26 x 16mm, 8 Degree, Tapered, Straight

    THERMO SCIENTIFIC MAS OMNI-IMMUNE, MAS OMNI IMMUNE PRO

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DEFENDER ROOM AIR CLEANER, MODEL RAC-4000A

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·September 12, 2019

    VITALITY

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013

    ACTIVA PC

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPEARTIONC CO., JUCNOS·Product code MHY·November 19, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 2, 2014