Duns Number:160061651
Device Description: The Vitrea Advanced Visualization software is a medical diagnostic system that allows the The Vitrea Advanced Visualization software is a medical diagnostic system that allows the processing, review, analysis, communication, and media interchange of multi-dimensional digital images acquired from a variety of imaging devices.The Vitrea Advanced Visualization system provides multi-dimensional visualization of digital images to aid clinicians in their analysis of anatomy and pathology. The Vitrea Advanced Visualization user interface follows typical clinical workflow patterns to process, review, and analyze digital images, including:• Retrieve image data over the network via DICOM• Display of images in dedicated protocols which are automatically adapted based on exam type• Select images for closer examination from a gallery of 2D or 3D views• Interactively manipulate an image in real-time to visualize anatomy and pathology• Annotate, measure, and record selected views• Output selected views to standard film or paper printers, or post a report to an intranet web server or export views to another DICOM device• Retrieve reports that are archived on a Web server
Catalog Number
-
Brand Name
Vitrea Advanced Visualization
Version/Model Number
7.12.2
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
JAK
Product Code Name
System, X-Ray, Tomography, Computed
Public Device Record Key
71c7618c-4153-4ba8-9988-baa6e294c720
Public Version Date
April 26, 2022
Public Version Number
2
DI Record Publish Date
April 14, 2020
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 38 |
2 | A medical device with a moderate to high risk that requires special controls. | 33 |