140 results · 7ms · 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.

Siemens brand MicroScan Dried Negative Breakpoint Combo 47 panels (B1017-417), SMN #: 10483099), For use in determining quantitative and/or qualitative antimicrobial agent susceptibility.

FDA Enforcement
Class II ·Terminated·Siemens Healthcare Diagnostics, Inc.·June 19, 2013

PASCAL and PASCAL Streamline (532 nm.577 nm); Treats the patient's eye.

FDA Enforcement
Class II ·Terminated·Topcon Medical Laser Systems, Inc·July 31, 2013

QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer designed for rapid thermalcycling and real-time detection of PCR assays.

FDA Enforcement
Class II ·Terminated·Qiagen Sciences LLC·March 18, 2020

OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Right, REF ZBH-PSNCRGH712-R.

FDA Enforcement
Class II ·Terminated·Orthosensor, Inc.·October 17, 2018

OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left, REF ZBH-PSNCRGH712-L.

FDA Enforcement
Class II ·Terminated·Orthosensor, Inc.·October 17, 2018

Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific Stretcher/Transfer Lift is used with Whirlpool or Aqua-Aire (air bubbling) bathing system intended for use in nursing homes, hospitals, and assisted living facilities to transfer and/or lift patients under the direct supervision of trained staff. Model 392000-1 is equipped with a scale.

FDA Enforcement
Class II ·Terminated·Penner Mfg Inc·April 1, 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

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