Microcatheters
Direxion HI-FLO
by Boston Scientific Corporation
A sterile, small-diameter, single-lumen, flexible tube designed for the controlled infusion of fluids (e.g., thrombolytics, diagnostic contrast media) into superselective small vessels (including intracranial, peripheral, or occluded coronary vasculature) for angiography/treatment, and typically also for the delivery of devices (e.g., embolization implants, guidewires) into tortuous vessels or across tight lesions. It may include an ultrasound transducer, a thermal sensor, and a hole for guidewire placement located at the distal tip. It is not a guide-catheter (i.e., is not intended to deliver other catheters or therapeutic leads directly through its lumen). This is a single-use device.
Direxion HI-FLO models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| M001195400 | — | Not stated | Available |
| M001195410 | — | Not stated | Available |
| M001195420 | — | Not stated | Available |
| M001195430 | — | Not stated | Available |
| M001195440 | — | Not stated | Available |
| M001195450 | — | Not stated | Available |
| M001195460 | — | Not stated | Available |
| M001195470 | — | Not stated | Available |
| M001195480 | — | Not stated | Available |
| M001195490 | — | Not stated | Available |
| M001195500 | — | Not stated | Available |
| M001195510 | — | Not stated | Available |
Procedures that use microcatheters
Frequently asked questions
What is Direxion HI-FLO used for?
A sterile, small-diameter, single-lumen, flexible tube designed for the controlled infusion of fluids (e.g., thrombolytics, diagnostic contrast media) into superselective small vessels (including intracranial, peripheral, or occluded coronary vasculature) for angiography/treatment, and typically also for the delivery of devices (e.g., embolization implants, guidewires) into tortuous vessels or across tight lesions. It may include an ultrasound transducer, a thermal sensor, and a hole for guidewire placement located at the distal tip. It is not a guide-catheter (i.e., is not intended to deliver other catheters or therapeutic leads directly through its lumen). This is a single-use device.
Who makes Direxion HI-FLO?
Direxion HI-FLO is made by Boston Scientific Corporation. It is listed under microcatheters in our device library.
What sizes does Direxion HI-FLO come in?
The FDA device database does not list sizes for Direxion HI-FLO. Check the instructions for use or ask a Boston Scientific Corporation representative.
Is Direxion HI-FLO MRI safe?
The FDA device database entry for Direxion HI-FLO does not state its MRI safety status. Check the labeling before MRI.
Is Direxion HI-FLO FDA cleared?
Direxion HI-FLO is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Boston Scientific Corporation sales representative?
Boston Scientific Corporation has not listed representatives on LA Vascular yet. Visit the Boston Scientific Corporation company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.