BEUDAMED
    8 results · 26ms · 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.

    SUBCUTANEOUS TUNNELING NEEDLES & HANDLES

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

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209128600·

    CIN AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    EDENTEC MODEL 2000W APNEA MONITOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BATTERY HANDPIECE/MODULAR FOR TRS

    FDA Adverse Event
    Malfunction ·N/I·Product code GEY·June 6, 2014

    ROTH NET PLATINUM

    FDA Adverse Event
    Malfunction ·UNITED STATES ENDOSCOPY GROUP, INC.·Product code KOG·November 28, 2012

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·September 30, 2010

    Exactech Equinoxe GLENOID,KEELED, CEMENTED, mates with 47, 50, 53 head, beta curvature, Sizes: a) Small, Item Number 314-02-02, b) Medium, Item Number 314-02-03, c) Large, Item Number 314-02-04, Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024