BEUDAMED
    8 results · 27ms · 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.

    BEAVER MULTIPURPOSE SAPPHIRE KNIFE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209115945·

    NEXUSTKO NEEDLELESS ACCESS DEVICE, MODEL NIS-5

    FDA 510(k)
    FDA Class 2 ·General Hospital

    dynaMX Tabbed Staple

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNSPECIFIED INSTRUMENT

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CTR·Product code HQE·April 2, 2014

    MYNX VASCULAR CLOSURE DEVICE 6F/7F

    FDA Adverse Event
    Injury ·ACCESSCLOSURE, INC.·Product code MGB·July 10, 2012

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 22, 2010

    Acumatch L-Series BIPOLAR LINER, 22mm (BIPOLAR ENDOPROSTHESIS-Hip), Item Numbers: a) 100-22-19, SZ. L; b) 100-22-20, SZ. M; c) 100-22-21, SZ. N; d) 100-22-22, SZ. P; e) 100-22-23, SZ. R; f) 100-22-24, SZ. S; g) 100-22-25, SZ. T

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