144 results
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7ms
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Sources: EU EUDAMED, US FDA
Tourni-Cot - Universal, UDI 00855364004085, Model Number TCU, Non-pneumatic Tourniquet - Product Usage: The device is intended to be used in surgery on fingers or toes to provide a blood-less field.
FDA Enforcement
Class II
·Terminated·Mar-Med Co·February 10, 2021
Civco, MTSR03 Shoulder Retractor with Wrist Loops Kit with Base, plus two pairs of wrist loops (nylon and sherpa), Non-sterile re-usable wool wrist strap, REF: 20SR03, Rx The devise is intended to pull patients shoulders down for clearance when treating lateral fields to the neck.
FDA Enforcement
Class II
·Terminated·Med Tec Inc·January 21, 2015
Merge PACS software. The firm name on the label is Merge Healthcare, Inc., Hartland, WI. Intended to create and display two-dimensional and three-dimensional images of anatomy from a series of digitally acquired images.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·August 17, 2016
Merge OfficePACS software. The firm name on the label is Merge Healthcare, Heartland, WI.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·July 20, 2016
Merge Cardio software. Product Usage: Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files or optical character recognition of measurements captured on images) and cardiology signal (waveform) data.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·March 29, 2017
Merge RadSuite software. Radiological image processing system.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·September 14, 2016
Merge Hemo software. Merge Hemo monitors, measures, and records physiologic data from a human patient undergoing a cardiac catheterization procedure. The Monitoring System is for the monitoring of vital parameters including ECG, SpO2, invasive blood pressure, temperature, NIBP and CO2, and for the evaluation of resting ECG, arrhythmias, ST-segments and cardiac output. Some systems are built and designed to measure End Tidal CO2. The system is intended for use in hospital cardiac catheterization laboratories
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·December 7, 2016
Mar Cor Purification Millenium HX Portable Reverse Osmosis System. Model 3025975. Product Usage: Water Purification System is intended to be used as a dialysis accessory to produce water through reverse osmosis for use with hemodialysis equipment..
FDA Enforcement
Class II
·Terminated·Mar Cor Purification·March 26, 2014
Merge Cardio software. The firm name on the label is Merge Healthcare, Hartland, WI. Intended to be used to acquire, store, print, transfer, and archive clinical information.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·May 31, 2017
RadSuite software. The firm name on the label is Merge Healthcare, Hartland, WI.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·August 31, 2016
Merge Cardio software. Product Usage: Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files or optical character recognition of measurements captured on images) and cardiology signal (waveform) data.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·January 25, 2017
Schiller AG ISA CO2 Sensor (AKA: PhaseIn Unit), Merge Part Number HW-HEMO-00001. The PhaseIn Unit is an optional accessory (sold separately) to the Merge Hemo Patient Data Module (PDM). The PDM is a major component of the Merge Hemo system.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·May 10, 2017
Merge OfficePACS software. The firm name on the label is Merge Healthcare, Hartland, WI. OfficePACS is intended for the manipulation and displaying of medical images by a suitable licensed and qualified healthcare professional. It can show images from different modalities and interfaces to various image storage and printing devices using DICOM or similar interface standards. OrthoPACS also uses such images, in conjunction with templates for prosthetic devices, for the purposes of choosing the nature and characteristics of the prosthetic device to be used when planning a potential surgical procedure.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·July 20, 2016
Merge Cardio software using EchoIMS. The firm name on the label is Merge Healthcare, Hartland, WI.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·March 29, 2017
Merge Cardio software.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·March 29, 2017
iConnect Enterprise Archive software.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·April 5, 2017
Merge Cardio software. Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files or optical character recognition of measurements captured on images) and cardiology signal (waveform) data.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·December 21, 2016
Civco, MTSR02 Shoulder Retractor with Sherpa Wrist Loops Kit with Base, Non-sterile re-usable wool wrist strap, REF: 20SR02SUB2, Rx Only, The devise is intended to pull patients shoulders down for clearance when treating lateral fields to the neck.
FDA Enforcement
Class II
·Terminated·Med Tec Inc·January 21, 2015
Merge Eye Care Systems, consisting of Merge Eye Station, Merge Eye Care PACS, and Merge Eye Station Import Utility (ESIU).
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·April 5, 2017
Merge OrthoPACS software.
FDA Enforcement
Class II
·Terminated·Merge Healthcare, Inc.·June 28, 2017