BEUDAMED
    6 results · 19ms · 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 ×

    R&D BATTERIES PART NOS. 5186 AND 5230

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    ESCOTEK-EST 221 VACUUM UNIT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BIOCLONES ELEGANCE LH ELISA KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CUB PEDIATRIC CRIB STRETCHER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FMS·February 5, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·ANIMAS CORP.·Product code LZG·December 21, 2010

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 18, 2014