CT Areta RT

Primary DI
00884838129542
Brand
CT Areta RT
Company
Philips Healthcare (Suzhou) Co., Ltd.
Model
CT Areta RT
Catalog number
728382
Device description
Computed Tomography X-Ray System is intended to produce images of the head and body by computer reconstruction of x-ray transmission data taken at different angles and planes. This device includes Data acquisition system, detection management system and an operating console with display monitors along with patient and system supporting devices, accessories and components.
Published
2026-04-03
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information

Contact Domains#

Product Codes#

Code, Name table
CodeName
JAKSystem, X-Ray, Tomography, Computed

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
JAKSystem, X-Ray, Tomography, ComputedRadiology2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00884838129542PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00884838129542008848381295428848381295420884838129542

GMDN Terms#

Term, Definition table
TermDefinition
Full-body CT systemAn assembly of diagnostic x-ray computed tomography (CT) devices with a gantry large enough to allow imaging of any part of the body. It includes designs with single or multiple fixed annular arrays of x-ray tubes and opposing detectors or those with x-ray tube(s) and opposing detector assemblies that rotate rapidly around a central axis point within the gantry imaging area. It can produce two and/or three-dimensional (3-D) cross-sectional (tomographic) images, including spiral CT or other special imaging applications at multiple specified angles in relation to body position. It may use a variety of digital techniques for information capture, image reconstruction, and display.

Contacts#

Phone, Email table
PhoneEmail
+86018911415886tiffany.zhang@philips.com

Regulatory Flags#

DUNS number
421265537
Device count
1
Serial number
true
Manufacturing date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00884838129528CT RembraCT Rembra7283832026-04-03
00884838129535CT Rembra RTCT Rembra RT7283812026-04-03
00884838085015Incisive CTIncisive CT7281432019-10-01
00884838096813dS TorsoCardiac 1.5TdS TorsoCardiac 1.5T45980168199X2022-04-17
00884838096837dS MSK M 1.5TdS MSK M 1.5T45980168201X2022-04-17
00884838113237CT 5300CT 53007282852024-11-11
00884838096820dS MSK S 1.5TdS MSK S 1.5T45980168200X2022-04-17
00884838105508Incisive CTIncisive CT7281442021-12-30
00884838095199DigitalDiagnost C50DigitalDiagnost C507122042020-09-04
00884838095205DuraDiagnostDuraDiagnost7122032020-09-04
00884838064737DuraDiagnost CompactDuraDiagnost Compact7122132016-09-23
00884838064751DuraDiagnostDuraDiagnost7122142016-09-23
00884838082366DigitalDiagnost C50DigitalDiagnost C507122012017-10-26

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