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FujiMedical Synapse Cardiovascular I ProSolv CardioVascular. A picture Archiving and Communication System Software versions: Synapse Cardiovascular v4.0.8 Synapse Cardiovascular v4.0.8 SR1

FDA Recall
Terminated ·Fujifilm Medical Systems U.S.A., Inc.·Product code DQK·February 4, 2015

MEDITECH Microbiology - Calculator/data processing module, for clinical use.

FDA Recall
Terminated ·Medical Information Technology, Inc.·Product code JQP·January 17, 2014

MEDITECH Microbiology - Calculator/data processing module, for clinical use.

FDA Enforcement
Class II ·Terminated·Medical Information Technology, Inc.·March 12, 2014

Merge Cardio software. The firm name on the label is Merge Healthcare, Hartland, WI. Image processing system.

FDA Enforcement
Class II ·Terminated·Merge Healthcare, Inc.·September 7, 2016

FujiMedical Synapse Cardiovascular I ProSolv CardioVascular. A picture Archiving and Communication System Software versions: Synapse Cardiovascular v4.0.8 Synapse Cardiovascular v4.0.8 SR1

FDA Enforcement
Class II ·Terminated·Fujifilm Medical Systems U.S.A., Inc.·May 20, 2015

McKesson Radiology 12.2 - Picture Archive Communication System (PACS)

FDA Enforcement
Class II ·Terminated·Mckesson Medical Imaging·March 8, 2017

Fujifilm Synapse Cardiovascular I ProSolv CardioVascular Synapse Cardiovascular v4.0.8 Synapse Cardiovascular v4.0.8 SR1 Intended Use: Picture Archiving and Communication System Computer, Diagnostic, Programmable

FDA Enforcement
Class II ·Terminated·Fujifilm Medical Systems U.S.A., Inc.·May 20, 2015

Case Cardiac Assessment System for Exercise Testing and CardioSoft Diagnostic System Exercise Stress Testing ECG application

FDA Enforcement
Class II ·Terminated·GE Healthcare, LLC·June 30, 2021

Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient information in a database, and it may analyze and/or display the data in different formats for evaluation by healthcare professionals for informational purposes.

FDA Enforcement
Class II ·Terminated·Picis Inc.·August 7, 2013

SoftLab Software Laboratory information system to be used in a medical research or clinical laboratory by knowledgeable, trained,

FDA Enforcement
Class II ·Terminated·Soft Computer Consultants, Inc.·August 9, 2017

MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR) used for oncology workflow management. It lets users supply electronic patient charts and assemble care plans, order diagnostic tests, and prescribe medications. It also lets users import, view, annotate, manipulate, enhance, manage, and archive images.

FDA Enforcement
Class II ·Terminated·Elekta, Inc.·November 7, 2012

Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the central programming, monitoring and power supply component for the Alaris System

FDA Enforcement
Class II ·Terminated·Carefusion Corporation·April 24, 2013

Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient information in a database, and it may analyze and/or display the data in different formats for evaluation by healthcare professionals for informational purposes.

FDA Recall
Terminated ·Picis Inc.·Product code NSX·June 21, 2013

Fujifilm Synapse Cardiovascular I ProSolv CardioVascular Synapse Cardiovascular v4.0.8 Synapse Cardiovascular v4.0.8 SR1 Intended Use: Picture Archiving and Communication System Computer, Diagnostic, Programmable

FDA Recall
Terminated ·Fujifilm Medical Systems U.S.A., Inc.·Product code DQK·February 4, 2015

McKesson Radiology 12.2 - Picture Archive Communication System (PACS)

FDA Recall
Terminated ·Mckesson Medical Imaging·Product code LLZ·December 2, 2016

00597001303 Femur CR PRC FEM COMP SIZE CML Rx, Sterile; 00597001304 Femur CR PRC FEM COMP SIZE CMR Rx, Sterile; 00597001403 Femur CR PRC FEM COMP SIZE DML Rx, Sterile; 00597001404 Femur CR PRC FEM COMP SIZE DMR Rx, Sterile; 00597001503 Femur CR PRC FEM COMP SIZE EML Rx, Sterile; 00597001504 Femur CR PRC FEM COMP SIZE EMR Rx, Sterile; Used in total knee arthroplasty and indicated for patients with severe pain.

FDA Enforcement
Class II ·Terminated·Zimmer, Inc.·August 28, 2013

00597201303 Femur CR POR FM COMP SIZE CML Rx, Sterile; 00597201304 Femur CR POR FM COMP SIZE CMR Rx, Sterile; 00597201403 Femur CR POR FM COMP SIZE DML Rx, Sterile; 00597201404 Femur CR POR FM COMP SIZE DMR Rx, Sterile; 00597201503 Femur CR POR FM COMP SIZE EML Rx, Sterile; 00597201504 Femur CR POR FM COMP SIZE EMR Rx, Sterile; Used in total knee arthroplasty and indicated for patients with severe pain.

FDA Enforcement
Class II ·Terminated·Zimmer, Inc.·August 28, 2013

00597201333 Femur CR POR SURF HDN FEM CO-NID CML, Rx, Sterile; 00597201334 Femur CR POR SURF HDN FEM CO-NID CMR, Rx, Sterile; 00597201433 Femur CR POR SURF HDN FEM CO-NID DML, Rx, Sterile; 00597201434 Femur CR POR SURF HDN FEM CO-NID DMR, Rx, Sterile; 00597201533 Femur CR POR SURF HDN FEM CO-NID EML, Rx, Sterile; 00597201534 Femur CR POR SURF HDN FEM CO-NID EMR, Rx, Sterile; Used in total knee arthroplasty and indicated for patients with severe pain.

FDA Enforcement
Class II ·Terminated·Zimmer, Inc.·August 28, 2013

65597201333 Femur CR POR FEM SURF HDN HATCP CML, Rx, Sterile; 65597201334 Femur CR POR FEM SURF HDN HATCP CMR, Rx, Sterile; 65597201433 Femur CR POR FEM SURF HDN HATCP DML, Rx, Sterile; 65597201434 Femur CR POR FEM SURF HDN HATCP DMR, Rx, Sterile; 65597201533 Femur CR POR FEM SURF HDN HATCP EML, Rx, Sterile; 65597201534 Femur CR POR FEM SURF HDN HATCP EMR, Rx, Sterile; Used in total knee arthroplasty and indicated for patients with severe pain.

FDA Enforcement
Class II ·Terminated·Zimmer, Inc.·August 28, 2013

00597001333 Femur CR PRC SURF HDN FEM CO-NID CML Rx, Sterile; 00597001334 Femur CR PRC SURF HDN FEM CO-NID CMR Rx, Sterile; 00597001433 Femur CR PRC SURF HDN FEM CO-NID DML Rx, Sterile; 00597001434 Femur CR PRC SURF HDN FEM CO-NID DMR Rx, Sterile; 00597001533 Femur CR PRC SURF HDN FEM CO-NID EML Rx, Sterile; 00597001534 Femur CR PRC SURF HDN FEM CO-NID EMR Rx, Sterile; Used in total knee arthroplasty and indicated for patients with severe pain.

FDA Enforcement
Class II ·Terminated·Zimmer, Inc.·August 28, 2013