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.

    SCLERAL SPONGE II, OLK DESIGN, E5395-10 & E5395-11

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209105182·KIT, ACTIVE SHOOTER RESPONSE - RED

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515224889·Dautrey-Munro Osteo, 10mm, 6 1/4"

    SAFERSLEEP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HyaloGYN Vaginal Hydrating Gel

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

    EXT SET 7IN REM CLAVE SITE NDEHP

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·February 12, 2014

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·November 15, 2012

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 28, 2010