9 results · 8ms · Sources: EU EUDAMED, US FDA

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Brilliance iCT SP Computed Tomography X-ray system

FDA Enforcement
Class II ·Terminated·Philips Medical Systems (Cleveland) Inc·December 30, 2015

Brilliance iCT SP Computed Tomography X-ray Systems, Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes

FDA Enforcement
Class II ·Terminated·Philips Medical Systems (Cleveland) Inc·April 20, 2016

Brilliance iCT SP - Model 728311 Brilliance iCT - Model 728306 Computed Tomography X-ray systems

FDA Enforcement
Class II ·Terminated·Philips Medical Systems (Cleveland) Inc·January 31, 2018

Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography and Computed Tomography System Model:uMI 550 MD, Rx Only

FDA Enforcement
Class II ·Ongoing·UIH Technologies LLC·October 29, 2025

iCT SP (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.

FDA Enforcement
Class II ·Terminated·Philips Medical Systems (Cleveland) Inc·June 17, 2015

Brilliance iCT and Brilliance iCT SP These systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. May include signal analysis and display equipment, patient and equipment supports, components and accessories

FDA Enforcement
Class II ·Terminated·Philips Medical Systems (Cleveland) Inc·February 5, 2014

Philips DigitalDiagnost C50 -intended for use in generating radiographic images of human anatomy Model Number : 712201

FDA Enforcement
Class II ·Ongoing·Philips North America Llc·April 19, 2023

Medrad Continuum MR Infusion system- non-wireless system The MEDRAD Continuum MR Infusion System is designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy directly prior to, during and immediately after the MR procedure functioning while either stationary or mobile. It is not intended to provide long-term patient care outside the MR environment. The system is to be used by trained medical staff, primarily critical care, emergency room and radiology nursing staff.

FDA Enforcement
Class II ·Terminated·Bayer Corp·June 11, 2014

Reamer / Irrigator / Aspirator (RIA): RIA Drive Shafts, RIA Tube Assemblies, sterile, RIA Reamer Head, sterile (12.0mm-19.0mm); intended to clear the medullary canal of bone marrow and debris and to effectively size the medullary canal for the acceptance of an intramedullary implant or prosthesis

FDA Enforcement
Class II ·Terminated·Synthes, Inc.·July 22, 2015