Broadway™ System
Made for the M1SSION
The Broadway System is a fully integrated stroke access solution. Each device is engineered to optimize the next for seamless access from groin to M1.
Individually strong.
Together,
unstoppable.
Broadway 8 Catheter's low profile 2.41mm distal outer diameter closely matches the average M1 diameter1 to deliver a reliable fit in more patients.2
1. ASSIST Registry
2. As compared to 0.088in super-bore catheters.
36OMax™ Laser Technology powers our super-bore access catheter platform, featuring thousands of laser cuts in a stainless steel hypotube.
The result? A large lumen, low-profile access catheter that delivers on trackability while maintaining lumen patency, kink resistance, and 8F closure compatibility.
That's innovation in action.
Broadway 8
Distal "helix" pattern
Echo Intracranial Base
Distal "trident" pattern
Dash Hydrophilic Short Sheath
Thin-wall, braided-reinforcement short sheath designed to fit our 9F system while maintaining the familiar workflow of an 8F closure.
| Inner diameter | Length |
| 0.126in / 3.20mm | 11cm |
Echo Intracranial Base Catheter
Engineered with our newest 36OMax laser technology, Echo provides a supportive base with a large 0.100in lumen for optimal delivery of Broadway 8.
| Inner diameter | Outer diameter | Length |
| 0.100in / 2.54mm | 0.118in / 3.00mm | 100cm and 105cm |
Broadway 8 Catheter
The 0.084in ID Broadway 8 Catheter, engineered with 36OMax Laser Technology, delivers the handling of a 0.070" ID catheter while offering a 44% larger lumen.
| Inner diameter | Outer diameter | Length |
| 0.084in / 2.13mm | Proximal: 0.098in / 2.49mm Distal: 0.095in / 2.41mm |
132cm |
FastPass Delivery Assist Catheter
Minimizes the ledge for smooth navigation of Broadway 8 Catheter into the M1.
| Inner diameter | Outer diameter | Length |
| 0.0165in / 0.42mm | Distal: 0.033in / 0.84mm Bulb: 0.075in / 1.91mm |
156cm |
Thank you!
This document is intended solely for the use of healthcare professionals.
A physician must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when treating a particular patient. Stryker does not dispense medical advice and recommends that physicians be trained in the use of any particular product before using it in a procedure. The information presented is intended to demonstrate the breadth of Stryker product offerings. A physician must always refer to the package insert, product label and/or instructions for use before using any Stryker product.
Products may not be available in all markets because product availability is subject to the regulatory and/or medical practices in individual markets. Please contact your Stryker representative if you have questions about the availability of Stryker products in your area.
AP004859 V1.0