Guidewires
Kendall
by Covidien LP
A sterile hand-operated device intended to be attached to the proximal end of an invasive device (e.g., a catheter, a needle, or a guidewire) to provide the operator with the ability to manually manipulate and control the directional torque (rotation) of the device to which it is attached. This device may be made of plastic or metal materials. This is a single-use device.
Find similar guidewires
Where to buy Kendall
Contact Covidien LP directly; they can quote, ship, or point you to the distributor for your country.
From medtronic.com, checked October 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
Kendall 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 |
|---|---|---|---|
| WWTD35001 | — | Not stated | Available |
| WWTD35001 | — | Not stated | Available |
FDA clearances
- 510(k) K120863 April 2012
Procedures that use guidewires
Frequently asked questions
What is Kendall used for?
A sterile hand-operated device intended to be attached to the proximal end of an invasive device (e.g., a catheter, a needle, or a guidewire) to provide the operator with the ability to manually manipulate and control the directional torque (rotation) of the device to which it is attached. This device may be made of plastic or metal materials. This is a single-use device.
Who makes Kendall?
Kendall is made by Covidien LP. It is listed under guidewires in our device library.
What sizes does Kendall come in?
The FDA device database does not list sizes for Kendall. Check the instructions for use or ask a Covidien LP representative.
Is Kendall MRI safe?
The FDA device database entry for Kendall does not state its MRI safety status. Check the labeling before MRI.
Is Kendall FDA cleared?
Kendall is covered by FDA submission K120863.
How do I contact a Covidien LP sales representative?
Covidien LP has not listed representatives on LA Vascular yet. Visit the Covidien LP 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.