Arrowg+ard Blue® MAC

Flow Meets Maximum Versatility

The Arrowg+ard Blue® MAC is designed to meet the needs of a variety of patient types — from trauma to cardiac. The catheter combines the access of a sheath introducer with the high-flow lumens of a central line. The MAC's hemostasis valve allows for easy access for additional devices, such as a thermodilution catheter or Arrow® MAC Companion Catheter adding up to three additional lumens. The 9 French distal lumen accommodates large fluid volumes when needed, while the 12-gauge proximal lumen provides a separate access for incompatible fluid administration.

Flow Rate Comparison by Vascular Device

IV1 PICC3 Intraosseous CVC3 Sheath
Introducer2
Mac3
1.2 - 6.3 1.6 6.3 3-6 12 29

Note: This table compares the highest flow lumen per vascular access device. PICC, CVC, Sheath Introducer and MAC flow rates are gravity saline flow rates. IV and Intraosseous flow rates are based off pressure bag flow rates, and they are provided by another manufacturer.

MAC Flow Rates

Lumen Flow
rate (ML/HR)3
Distal (9 Fr.) No Catheter 29,920
Distal (9 Fr.) with 8 Fr. Catheter 12,180
Distal (9 Fr.) with 7 Fr. Catheter 19,810
Proximal (12 Ga.) No Catheter 9,340

Based on 100 cm head height gravity saline flow rates. Flow rates would be higher with a rapid infuser or pressure bag.

The Arrow® MAC uses proprietary chlorhexidine-based antimicrobial protection designed to protect your patients from the known pathogens of Catheter-Related Bloodstream Infections (CRBSIs).


Now available in Arrow® ErgoPack® Complete System kit configurations

VA-Ergopack-Complete

Arrow® ErgoPack® Complete systems put necessary components in an intuitive configuration to help optimize your workflow, comply with CDC, SHEA, INS, and OSHA guidelines3-6, and fight against central line-associated bloodstream infections(CLABSI).

Check out what’s new:

Arrow GlideWheel Advancer

Arrow GlideWheel™ Advancer

Provides tactile feedback + finer control

Nitinol Wire

Nitinol wire

Is kink-resistant compared to stainless steel

Transducer cover

Transducer cover

To support guidelines for ultrasound insertion

Syringes

Pre-filled sterile saline syringe

One pre-filled sterile saline syringe per lumen now included inside the kit

ChloraPrep applicators

Extra ChloraPrep® Skin Prep

Extra applicator now included in each kit

References:

  1. Pressure Injectable VANTEX Central Venous Catheters Indications For Use.  Williamston, MI:  Centurion Medical Products; 4.

  2. Gupta N, Weber H, Moss S, Gaire-Patel K. Are antibiotic resistant “super bugs” a real challenge to antimicrobial central venous catheter performance? AVA 2014.

  3. O'Grady NP, Alexander M, Burns LA, et al. Guidelines for the Prevention of Intravascular Catheter-Related Infections, 2011 (Revised 2017). 2. Atlanta, GA: Centers for Disease Control and Prevention; 2017.

  4. Buetti, N., Marschall, J., Drees, M., Fakih, M., Hadaway, L., Maragakis, L., . . . Mermel, L. (2022). Strategies to prevent central line-associated bloodstream infections in acute-care hospitals: 2022 Update. Infection Control & Hospital Epidemiology, 1-17. doi:10.1017/ice.2022.87

  5. Gorski L, Hadaway L, Hagle ME, McGoldrick M, et al. Infusion Therapy Standards of Practice. Journal of Infusion Nursing. 2016; Jan 39(1S).

  6. Occupational Safety & Health Administration Regulations (Standards – 29 CFR). Part 1910.1030: Bloodborne pathogens. Occupational Safety & Health Administration Web site. https://www.osha.gov/laws-regs/regulations/standardnumber/1910/1910.1030. Accessed on February 12, 2020.



Contraindication:
The Arrowg+ard Blue® MAC is contraindicated for patients with known hypersensitivity to chlorhexidine and silver sulfadiazine and/or sulfa drugs.

Federal Law (USA) restricts these devices to sale by or on the order of a physician.

Teleflex, the Teleflex logo, and Arrow, Arrowg+ard Blue, and ErgoPack are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries. All other trademarks are the trademarks of their respective owners. Please check your local regulatory approval status. Refer to the applicable Instructions for Use for the indications approved in your geography.

Information in this material is not a substitute for the product Instructions for Use. This document does not imply compatibility between devices. Not all products may be available in all countries. Please contact your local representative. Revised: 08/2022. ©2022 Teleflex Incorporated. All rights reserved. MC-007978 LA EN