BEUDAMED
    8 results · 28ms · 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 ×

    PENNINE DERBY YANKAUER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209107384·KIT, SQUAD

    Disposable Infusion Bag for Parenteral Nutrition

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PINNACLE CONSTRAINED ACETABULAR LINERS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTRACLUDE

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DXC·June 5, 2014

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 4, 2010

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 30, 2012

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020