Microcatheters
Tracker-17
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.
Tracker-17 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 |
|---|---|---|---|
| M003TMC0750 | Length 150.0 cm | MR Conditional | Available |
| M003TMC1500 | Length 150.0 cm | MR Conditional | Available |
Procedures that use microcatheters
Frequently asked questions
What is Tracker-17 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 Tracker-17?
Tracker-17 is made by Stryker Corporation. It is listed under microcatheters in our device library.
What sizes does Tracker-17 come in?
Sizes listed for Tracker-17: Length: 150 cm. Confirm availability with the manufacturer's instructions for use.
Is Tracker-17 MRI safe?
The FDA device database lists Tracker-17 as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Tracker-17 FDA cleared?
Tracker-17 is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Stryker Corporation sales representative?
Stryker Corporation has not listed representatives on LA Vascular yet. Visit the Stryker 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.