BEUDAMED
    39 results · 24ms · 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 ×

    OMRON FAT LOSS MONITOR WITH SCALE, MODEL HBF-400

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K0430200·Sagittal Bender, Double Ended Left

    APOLLO Ankle Fracture Plating System

    FDA UDI
    Glw, Inc.·18435711004204·APOLLO Ankle Fracture Plates / 4.3mm / Non-Lock...

    PLASMAKINETIC GENERATOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ICS MEDICAL MODEL VG-30 VIDEO GOGGLES

    FDA 510(k)
    FDA Class 2 ·Neurology

    ARROW CVC SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DQY·April 9, 2021

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 15, 2013

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 15, 2013

    ARROW CVC SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL LLC·Product code DQY·November 11, 2022

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

    ARROW CVC KIT: 5-LUMEN 8.5FR X 16CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL LLC·Product code FOZ·March 21, 2022

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

    ARROW CVC SET: 16 GA X 8" (20 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL LLC·Product code DQY·September 21, 2022

    GRIPPER MICRO SAFETY NEEDLE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD (FORMERLY DELTEC, INC)·Product code FPA·March 15, 2013

    PENUMBRA COIL 400

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code KRD·February 24, 2011

    CONTAK RENEWAL 3 RF

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014

    ARROW CVC SET: 16 GA X 8" (20 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL LLC·Product code FOZ·May 10, 2022

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014