gudid Primary ID: CT Areta RT

CT Areta RT (UDI CT Areta RT)

Manufactured by Philips Healthcare (Suzhou) Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The CT Areta RT (Model/Catalog Number: CT Areta RT) is a medical device manufactured by Philips Healthcare (Suzhou) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification JAK within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1003-2026 View Full Alert →

Philips Incisive CT...

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ID: Z-1273-2021 View Full Alert →

Philips CT systems are advanced continuous-rotation computed tomography systems suitable for a wide range of computed tomographic (CT) appli...

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ID: Z-0640-2024 View Full Alert →

Incisive CT, model 728143 & 728144 running Software Version 5.0.0....

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Technical Specifications

Model Number: CT Areta RT
Product Code / EMDN: JAK
Device Name: 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.
Database Sync Date: 2026-08-09 09:45:39

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of CT Areta RT?

The registered manufacturer of record for CT Areta RT is Philips Healthcare (Suzhou) Co., Ltd..

What is the Primary UDI-DI identifier for CT Areta RT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CT Areta RT.

What classification code is assigned to this device?

This device is registered under product classification code JAK.

Similar Classification Devices (JAK)

Other Devices by Philips Healthcare (Suzhou) Co., Ltd.

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