Angiographic catheters
Lehman
A thin, flexible tube designed to inject a contrast medium into select blood vessels of the cerebral, visceral, or peripheral vasculature during an angiographic procedure in order to facilitate the clear visualization of the vascular system of a targeted organ or area of the body. It is introduced percutaneously, has a radiopaque marker(s) for positioning, and may include disposable devices dedicated to catheter introduction/function [e.g., sheath(s)]. It may also be used for simultaneous pressure measurements to determine the transvalvular, intravascular, and intraventricular pressure gradients. This is a single-use device.
Lehman 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 |
|---|---|---|---|
| 001253 | Catheter Gauge 5.0 Fr; Lumen/Inner Diameter 0.889 mm; Length 50.0 cm | Not stated | Available |
| 001253 | Length 50.0 cm; Lumen/Inner Diameter 0.889 mm; Catheter Gauge 5.0 Fr | Not stated | Available |
| 001254 | Lumen/Inner Diameter 0.889 mm; Catheter Gauge 5.0 Fr; Length 80.0 cm | Not stated | Available |
| 001254 | Length 80.0 cm; Lumen/Inner Diameter 0.889 mm; Catheter Gauge 5.0 Fr | Not stated | Available |
| 001259 | Length 100.0 cm; Lumen/Inner Diameter 1.194 mm; Catheter Gauge 6.0 Fr | Not stated | Available |
| 001259 | Lumen/Inner Diameter 1.194 mm; Catheter Gauge 6.0 Fr; Length 100.0 cm | Not stated | Available |
| 001260 | Lumen/Inner Diameter 1.194 mm; Length 125.0 cm; Catheter Gauge 6.0 Fr | Not stated | Available |
| 001260 | Catheter Gauge 6.0 Fr; Length 125.0 cm; Lumen/Inner Diameter 1.194 mm | Not stated | Available |
| 001263 | Lumen/Inner Diameter 1.499 mm; Catheter Gauge 7.0 Fr; Length 100.0 cm | Not stated | Available |
| 001263 | Catheter Gauge 7.0 Fr; Length 100.0 cm; Lumen/Inner Diameter 1.499 mm | Not stated | Available |
| 001264 | Length 125.0 cm; Lumen/Inner Diameter 1.499 mm; Catheter Gauge 7.0 Fr | Not stated | Available |
| 001264 | Catheter Gauge 7.0 Fr; Lumen/Inner Diameter 1.499 mm; Length 125.0 cm | Not stated | Available |
| 001267 | Catheter Gauge 8.0 Fr; Length 125.0 cm; Lumen/Inner Diameter 1.753 mm | Not stated | Available |
| 001267 | Length 125.0 cm; Catheter Gauge 8.0 Fr; Lumen/Inner Diameter 1.753 mm | Not stated | Available |
| 990101 | Length 80.0 cm; Lumen/Inner Diameter 1.194 mm; Catheter Gauge 6.0 Fr | Not stated | Available |
| 990101 | Catheter Gauge 6.0 Fr; Lumen/Inner Diameter 1.194 mm; Length 80.0 cm | Not stated | Available |
Procedures that use angiographic catheters
Frequently asked questions
What is Lehman used for?
A thin, flexible tube designed to inject a contrast medium into select blood vessels of the cerebral, visceral, or peripheral vasculature during an angiographic procedure in order to facilitate the clear visualization of the vascular system of a targeted organ or area of the body. It is introduced percutaneously, has a radiopaque marker(s) for positioning, and may include disposable devices dedicated to catheter introduction/function [e.g., sheath(s)]. It may also be used for simultaneous pressure measurements to determine the transvalvular, intravascular, and intraventricular pressure gradients. This is a single-use device.
Who makes Lehman?
Lehman is made by Medtronic, Inc.. It is listed under angiographic catheters in our device library.
What sizes does Lehman come in?
Sizes listed for Lehman: Lumen/Inner Diameter: 0.89–1.75 mm; Length: 50–125 cm; Catheter Gauge: 5–8 Fr. Confirm availability with the manufacturer's instructions for use.
Is Lehman MRI safe?
The FDA device database entry for Lehman does not state its MRI safety status. Check the labeling before MRI.
Is Lehman FDA cleared?
Lehman is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Medtronic, Inc. sales representative?
Medtronic, Inc. has not listed representatives on LA Vascular yet. Visit the Medtronic, Inc. 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.