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MEDRAD Centargo CT Injection System +4 more models

FDA 510(k)FDA UDIEUDAMED

Class II (US FDA 510(k))

510(k) K252689Ref CENT-DS

by Imaxeon Pty Ltd

Identity

Trade Name
MEDRAD® Centargo Day Set EUDAMEDFDA UDI
Generic Name
Angiographic syringe FDA UDI
Device Name
MEDRAD® Centargo Disposables EUDAMED
Centargo, KIT, SYR,CT, DAYSET, MC, US FDA UDI
Model / Reference
CENT-DS EUDAMEDFDA UDI
Description
Centargo, KIT, SYR,CT, DAYSET, MC, US FDA UDI

Identifiers

Catalog Number
CENT-DS FDA UDI
Primary DI / UDI-DI
09345390002335 EUDAMED
09345390003097 FDA UDI
Basic UDI-DI
934539000TFCN-0100UQ EUDAMED
510(k) Number
K252689 FDA 510(k)
FDA Product Code
IZQ FDA 510(k)FDA UDI
DXT FDA UDI
EMDN Code
A02010401 SYRINGES FOR CONTRAST MEDIA INJECTOR, SINGLE-USE EUDAMED
GMDN Term
Angiographic syringe FDA UDI
Models / Variants
MEDRAD Centargo CT Injection System FDA 510(k)FDA UDIEUDAMED
MEDRAD Centargo Day Set FDA 510(k)FDA UDIEUDAMED
MEDRAD Centargo Patient Line FDA 510(k)FDA UDIEUDAMED
MEDRAD Centargo Replacement Spike FDA 510(k)FDA UDIEUDAMED
MEDRAD ISI2 Module (ISI2) FDA 510(k)FDA UDIEUDAMED

Classification

Device Class
Class IIa EUDAMED
Class II FDA 510(k)FDA UDI
Legislation / Framework
21 CFR Part 870.1650 FDA 510(k)
Regulation Number
870.1650 FDA 510(k)FDA UDI
Market of Registration
Netherlands EUDAMED
Advisory Committee
Cardiovascular FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

The MEDRAD Centargo CT Injection System is an Automatic Injector for Contrast Medium, designed to deliver intravenous contrast agents during computed tomography (CT) scans. It ensures precise, programmable infusion rates to enhance image quality and diagnostic accuracy in cardiovascular and other CT imaging procedures. The system integrates with compatible CT scanners to automate contrast delivery, reducing operator variability and improving workflow efficiency.

This device is supplied as a reusable system with single-use consumables, including the Day Set, Patient Line, and Replacement Spike, which are intended for one-time use. The MEDRAD ISI2 Module (ISI2) is a key component for injection control and monitoring. The system is classified as Class II under FDA regulations and has received FDA 510(k) clearance and MDR authorization. It is intended for use in clinical settings where contrast-enhanced CT imaging is performed, adhering to standard sterility and safety protocols for medical imaging devices.

Frequently asked questions

What types of consumables are included with the MEDRAD Centargo CT Injection System, and how are they used?

The MEDRAD Centargo CT Injection System includes single-use consumables such as the Day Set, Patient Line, and Replacement Spike, which are designed for one-time use per patient. These components connect to the reusable injector system to deliver intravenous contrast agents during CT scans, ensuring sterile and contamination-free administration. The Day Set is likely a pre-assembled set of tubing and connectors, while the Patient Line and Replacement Spike provide flexibility for different patient needs or setup configurations.

Is the MEDRAD Centargo CT Injection System reusable, and if so, what maintenance or cleaning requirements should be considered?

Yes, the MEDRAD Centargo CT Injection System itself is reusable, while its consumables (Day Set, Patient Line, Replacement Spike) are single-use. Since it is a reusable device, proper cleaning, disinfection, and maintenance per manufacturer guidelines are essential to ensure reliability, sterility, and longevity. The system’s reusable components, such as the ISI2 Module, must be handled according to the manufacturer’s instructions to avoid cross-contamination and maintain performance for repeated use in clinical settings.

How does the MEDRAD Centargo CT Injection System integrate with CT scanners, and what makes its infusion control unique?

The MEDRAD Centargo CT Injection System is designed to integrate with compatible CT scanners to automate the delivery of intravenous contrast agents during imaging. Its infusion control is managed by the MEDRAD ISI2 Module (ISI2), which allows for precise, programmable infusion rates tailored to specific CT protocols. This automation reduces operator variability, enhances image quality, and improves workflow efficiency—particularly valuable in cardiovascular and other contrast-enhanced CT procedures where timing and dosage accuracy are critical.

What regulatory pathways has the MEDRAD Centargo CT Injection System followed, and how does this affect its use in clinical settings?

The system has undergone FDA 510(k) clearance and holds MDR (Medical Device Regulation) authorization, confirming its compliance with stringent safety and performance standards. These regulatory pathways ensure that the device meets requirements for Class II classification under FDA regulations and adheres to European medical device directives. Clinically, this means the system is validated for use in settings where contrast-enhanced CT imaging is performed, with adherence to standard sterility and safety protocols already established by regulatory bodies.

This description and any FAQs above were generated automatically from registry data and have not been verified by the manufacturer or by deviCERTS. Always check the official registry entry and the manufacturer's instructions for use before relying on them.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

MDR

United States Active

FDA_510K

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Manufacturer

Manufacturer
Imaxeon Pty Ltd
FDA Applicant
Imaxeon Pty, Ltd.

Sources (3)

  • FDA 510(k) K252689 24 fields · synced Sep 18, 2026
  • FDA UDI 686e886b-e419-4538-8938-616b2c55c042 37 fields · synced May 30, 2026
  • EUDAMED 72c3c770-cdb6-48cf-b0ae-8cd56e1460d8 61 fields · synced Jul 11, 2026