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.
    Filters Regulation: Us FDA ×

    MICROLIFE IT2CA1

    FDA 510(k)
    FDA Class 2 ·General Hospital

    320 P37,SY,2L,STKR

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828100205·320 P37,SY,2L,STKR

    DSL-10-2000 ACTIVE® CORTISOL ENZYME IMMUNOASSAY (EIA) KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code CGR·July 21, 2009

    Aquas Probes

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AZUR DETACTABLE 18, MODELS 45-480305, 45-480310, 45-480405, 44-480415

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·March 5, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    ATTAIN ABILITY

    FDA Adverse Event
    Malfunction ·MPRI·Product code OJX·August 7, 2014