BEUDAMED
    15 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.

    DIAMATIC, AUTOMATIC INSULIN INJECTOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PFC* MOD PLUS TORQUE DRIVER

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC 1818910·Product code HWR·February 13, 2018

    P.F.C.

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295215868·P.F.C. MODULAR PLUS TORQUE DRIVER

    PFC* MOD PLUS TORQUE DRIVER

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HWR·April 19, 2021

    CRYOCHECK CLOT APCR

    FDA 510(k)
    FDA Class 2 ·Hematology

    JointPoint

    FDA 510(k)
    FDA Class 2 ·Radiology

    PFC* MOD PLUS TORQUE DRIVER

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC 1818910·Product code HWR·February 28, 2018

    SIG HP REV TORQ LMT SCRWDRVR

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND - 9616671·Product code HXX·April 19, 2021

    SELECTSECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVN·June 10, 2014

    C-FLEX POLAR HEAD POSITIONER

    FDA Adverse Event
    Other ·ALLEN MEDICAL·Product code FWZ·November 28, 2012

    84" ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·VYGON·Product code FPA·September 22, 2010

    Philips PageWriter Touch Cardiograph, Model: 860284, Philips Medical Systems, Andover, MA, 01810

    FDA Recall
    Terminated ·Philips Medical Systems·Product code DPS·September 12, 2007

    MBT REV TIB 2 DEG BROACH 37MM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HTQ·April 19, 2021

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020

    OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.

    FDA Enforcement
    Class I ·Terminated·GE OEC Medical Systems, Inc·August 1, 2012