MEDRAD® Mark 7 Arterion
Brings confidence and convenience to your interventional and diagnostic procedures.
Clear Direction. Ergonomics, Convenience, and Reliability. MEDRAD® Mark 7 Arterion has stylish ergonomics designed to increase mobility around a busy lab. Less time positioning and setting up the system means more time for the patient. The convenient front-load syringe design and MEDRAD® Twist & Go disposable syringe provide optimized pre- and post-procedure work flow.
What is MEDRAD® Mark 7 Arterion?
MEDRAD® Mark 7 Arterion is a single-head injection system for X-ray angiography designed for high-end interventional radiology (IR) suites.
How does MEDRAD® Mark 7 Arterion work?
MEDRAD® Mark 7 Arterion allows the controlled delivery of radiopaque contrast media for interventional imaging purposes in interventional radiology, interventional cardiology and vascular surgery. The injector facilitates contrast delivery in fixed flow mode and variable flow with an optional software upgrading. It utilizes a dedicated 150 cc syringe (front load) and can deliver contrast media in phased mode.
What are MEDRAD® Mark 7 Arterion System Configurations and Main Components?
The MEDRAD® Mark 7 Arterion Injection System consists of three main components: Injector Head, Display Control Unit, and Power Supply. They are mounted with various options.
- Pedestal Configuration
The pedestal configuration combines all required injector components into an integrated, mobile unit
- Table Mount Configuration
This configuration option positions the injector head on the patient table, the DCU in the control room and the PS in the equipment (electronics) room
- Overhead Counterpoise System Configuration
The injector head can also be attached to an OCS system. Several versions accommodate most lab layouts
- MEDRAD® Mark 7 Arterion Dual Display Option
This option provides added flexibility allowing programming and control of the injector from two locations
How is MEDRAD® Mark 7 Arterion used?
The system is intuitively managed via the color touch screen DCU. All relevant information is displayed on the home screen where injection parameters can be programmed or changed. On the protocol screen up to 40 protocols can be stored, changed, deleted, or selected. A history tab allows to review the last 50 injections.
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| Standard: IEC 60601-1 |
IEC 60601-1 (2nd and 3rd edition Amendment 1) Medical electrical equipment, Part 1: General requirements for basic safety and essential performance |
|---|---|
| Standard: IEC 60601-1-2 |
Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests |
| Size and mobility |
Footprint: 66.2 cm x 55.9 cm (26.1 in. x 22.0 in.) Weight: 146 lbs. (66.22 kg) |
| Flow Rates |
60 mL: 0.1-45.0 mL/s in 0.1 mL/s increments (single and phased) 0.1-59.9 mL/m in 0.1 mL/m increments (single mL/m) 150-200 mL: 1.0-10.0 mL/s in 0.1mL/s increments (variable) |
| Volume | 150 mL |
| Pressure Limits |
60 mL: 100-1200 psi in 1 psi increments 200 mL: 689-8273 kPa in 1 kPa increments |
| Rise Time | 0.0-9.9 seconds in 0.1s increments |
| Delay Time | 0.0-99.9 seconds in 0.1s increments |
| Fill Speed |
Manual: 1-20 mL/s in 1 mL/s increments Automatic: 1-10 mL/s in 1 mL/s increments |
| Syringe Size | 150 mL |
| Memory |
Protocol: 39 Protocols (4 default, 35 storable) Injection History: Approximately 50 injections |
| Flow Rate Accuracy |
The Head shall inject fluid with a flow rate accuracy of ± (5% of programmed flow rate+0.25ml/s) in mL/s range as measured over 1 second, or 10mL, whichever is greater, while in fixed flow mode. The Head shall inject fluid with a flow rate accuracy of ± (5% of programmed flow rate +0.25mL/m) in mL/m range as measured over 4 seconds or 1mL, whichever is greater. The Head shall inject fluid with a flow rate accuracy of +/- (20% of the programmed flow rate +0.25mL/s) multiplied by the percentage commanded by the hand controller, while in variable flow mode. |
| Volume Accuracy | The Head shall deliver the programmed volume with an accuracy of ± (1.5% of programmed volume+2mL) in mL. |
| Standard IEC 60601-1: | IEC 60601-1:2005+Amendment 1:2012* Medical electrical equipment, Part 1: General requirements for basic safety and essential performance |
| Standard IEC 60601-1-2: | IEC 60601-1-2:2014** Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests |
**Arterion has been designed and tested in accordance with the most recent medical equipment electromagnetic compatibility standard. This ensures Arterion is well suited for the current medical device environment.
*Arterion has been designed and tested in accordance with the most recent medical equipment safety standard. This ensures Arterion is well suited for the current medical device environment.
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Senaste uppdatering: 03/2024
- PP-M-MARK-SE-0005-1
