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 ×

    K-ASSAY APO A1/B CALIBRATOR SET

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993606·anteriors; shade BL3; mould BIS

    Y-Knot OneStep Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·March 7, 2013

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 26, 2011

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·August 8, 2014