Guidewires
POINTER Nitinol Guidewire
by Argon Medical Devices, Inc.
A non-dedicated metal wire designed to position a catheter or similar interventional device (e.g., a dilator or an endoscope) within a lumen of the gastrointestinal (GI) tract, the tracheobronchial tree, and the urinary tract (i.e., not dedicated to either clinical application). Typically, the catheter is advanced over the wire after the wire has been manoeuvred to a treatment site (e.g., site of stent-placement). It is available in a variety of diameters and lengths, may have fluoroscopic markers, or be fitted with an introducer for entering the working channel of the catheter or other interventional device. This is a single-use device.
POINTER Nitinol Guidewire 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 |
|---|---|---|---|
| 180418210 | — | Not stated | Available |
| 180418260 | — | Not stated | Available |
| 180418300 | — | Not stated | Available |
FDA clearances
- 510(k) K031442 August 2003
Procedures that use guidewires
Frequently asked questions
What is POINTER Nitinol Guidewire used for?
A non-dedicated metal wire designed to position a catheter or similar interventional device (e.g., a dilator or an endoscope) within a lumen of the gastrointestinal (GI) tract, the tracheobronchial tree, and the urinary tract (i.e., not dedicated to either clinical application). Typically, the catheter is advanced over the wire after the wire has been manoeuvred to a treatment site (e.g., site of stent-placement). It is available in a variety of diameters and lengths, may have fluoroscopic markers, or be fitted with an introducer for entering the working channel of the catheter or other interventional device. This is a single-use device.
Who makes POINTER Nitinol Guidewire?
POINTER Nitinol Guidewire is made by Argon Medical Devices, Inc.. It is listed under guidewires in our device library.
What sizes does POINTER Nitinol Guidewire come in?
The FDA device database does not list sizes for POINTER Nitinol Guidewire. Check the instructions for use or ask a Argon Medical Devices, Inc. representative.
Is POINTER Nitinol Guidewire MRI safe?
The FDA device database entry for POINTER Nitinol Guidewire does not state its MRI safety status. Check the labeling before MRI.
Is POINTER Nitinol Guidewire FDA cleared?
POINTER Nitinol Guidewire is covered by FDA submission K031442.
How do I contact a Argon Medical Devices, Inc. sales representative?
Argon Medical Devices, Inc. has not listed representatives on LA Vascular yet. Visit the Argon Medical Devices, 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.