Medis Suite MRCT

Primary DI
B141MEDISSUITEMRCT20220
Brand
Medis Suite MRCT
Company
Medis Medical Imaging Systems B.V.
Model
2022
Device description
Medis Suite MRCT 2022 is indicated for use in clinical settings where more reproducible than manually derived quantified results are needed to support the visualization and analysis of MR and CT images of the heart and blood vessels for use on individual patients with cardiovascular disease. Further, Medis Suite MRCT 2022 allows the quantification of T2* in MR images of the heart and the liver. Finally, Medis Suite MRCT 2022 can be used for the quantification of cerebral spinal fluid in MR velocity-encoded flow images. When the quantified results provided by Medis Suite MRCT 2022 are used in a clinical setting on MR and CT images of an individual patient, they can be used to support the clinical decision making for the diagnosis of the patient. In this case, the results are explicitly not to be regarded as the sole, irrefutable basis for clinical diagnosis, and they are only intended for use by the responsible clinicians.
Published
2022-05-16
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
LLZSystem, Image Processing, Radiological

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LLZSystem, Image Processing, RadiologicalRadiology2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B141MEDISSUITEMRCT20210PreviousHIBCC0
B141MEDISSUITEMRCT20220PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Laboratory instrument/analyser application software IVDAn in vitro diagnostic software program intended to be used with an instrument/analyser (e.g., microscope slide digital imaging scanner, immunoassay analyser, real-time PCR machine), or a data management device connected to the instrument/analyser, to: 1) facilitate user-controlled device function [e.g., incubation control]; 2) assist data processing, display, or communication [e.g., image conversion]; and/or 3) produce raw-data-derived qualitative result calculations based on specified criteria [positive or negative assay result]. This software does not use demographic or clinical data to produce a patient score (i.e., it is not interpretive).

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
549961191
Device count
1
Serial number
true
Manufacturing date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
B141MEDISSUITEMRCT20260Medis Suite MRCT20262026-09-25
B141QIVUS300QIvus3.02026-04-21
B141MEDISSUITEMRCT20250Medis Suite MRCT20252025-05-14
B141MEDISSUITEMRCT20230Medis Suite MRCT20232023-06-05
B141MEDISSUITEXA20230Medis Suite XA20232023-06-05
B141MEDISSUITEXA20220Medis Suite XA20222022-05-16
B141MEDISSUITEMRCT20190Medis Suite MRCT20192020-01-28
B141MEDISSUITEMRCT300Medis Suite MRCT3.02017-08-07
B141MEDISSUITEMRCT20210Medis Suite MRCT20212021-10-11
B141MEDISSUITEXA20210Medis Suite XA20212021-10-11
B141MEDISSUITEMRCT20200Medis Suite MRCT20202020-09-11
B141MEDISSUITEXA20200Medis Suite XA20202020-09-11
B141MEDISSUITEXA2D20190Medis Suite XA 2D20192020-02-20
B141MEDISSUITEXA20190QAngio XA 3D2.02020-01-28
B141MEDISSUITEMRCT20180Medis Suite MRCT20182018-08-07
B141MEDISSUITEMRCT210Medis Suite MRCT2.12017-03-06
B141MEDISSUITEXA2D20180Medis Suite XA 2D20182018-08-07
B141QANGIOXA730QAngio XA7.32016-06-13

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Primary DI, Brand, Company table
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