BEUDAMED
    7 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.
    Filters Regulation: Us FDA ×

    EXTENSION SETS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    NexxZr Plus Multi 2.0 B1 W98-20mm

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271158642·

    Precision Screw

    FDA 510(k)
    FDA Class 2 ·Neurology

    EMIT 2000 TACROLIMUS ASSAY AND SAMPLE PRETREATMENT REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 21, 2014

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·September 26, 2012

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 13, 2010