BEUDAMED
    36 results · 23ms · 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 ×

    DynamicIQ

    FDA 510(k)
    FDA Class 2 ·Radiology

    SELECTOR 24 KHZ NEURO SHORT HANDPIECE

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES, LTD.·Product code LFL·October 18, 2010

    ELCAM STOPCOCKS AND MANIFOLDS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Paragon 28 External Ring Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SELECTOR 24 KHZ MICRO HANDPIECE

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES, LTD.·Product code LFL·October 18, 2010

    1222895-2015-00029

    FDA Adverse Event
    Malfunction ·July 8, 2015

    200 MICRON TFL SINGLE USE FIBER

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code GEX·February 8, 2023

    HEAD RING POST

    FDA Adverse Event
    Malfunction ·INTEGRA BURLINGTON, MA, INC.·Product code HAW·March 11, 2015

    YUME SET FOR UV FLASH

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 2, 2010

    HR-IM INTUBATION HR ASSEMBLY

    FDA Adverse Event
    Malfunction ·INTEGRA RADIONICS, INC.·Product code HAW·January 4, 2011

    NEUROSIGHT ARC ON LAPTOP

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HAW·January 13, 2016

    MLX 300W XENON LIGHTSOURCE

    FDA Adverse Event
    Malfunction ·INTEGRA BURLINGTON, MA. INC.·Product code FCW·October 9, 2014

    SELECTOR 24KHZ MICRO STERILE TIP & FLUE SET X 5

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES, LTD.·Product code GEI·November 30, 2009

    PHANTOM BASE ASSEMBLY

    FDA Adverse Event
    Malfunction ·INTEGRA BURLINGTON, MA, INC.·Product code HAW·August 21, 2014

    UCHR ASSEMBLY

    FDA Adverse Event
    Malfunction ·INTEGRA RADIONICS, INC.·Product code HAW·October 17, 2006

    CRW MAYFIELD ADAPTOR

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HAW·January 12, 2016

    CUSA NXT SERVICE MODULE (115V)

    FDA Adverse Event
    Malfunction ·INTEGRA RADIONICS, INC.·Product code LFL·October 6, 2010

    NEUROSIGHT ARC ON LAPTOP

    FDA Adverse Event
    Malfunction ·INTEGRA, BURLINGTON·Product code HAW·October 14, 2011

    RADIAL JAW 3 BIOPSY FORCEPS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FCL·November 6, 2008

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·August 10, 2011