Guidewires
WallStent
by Lake Region Medical Limited
A metal coil or wire intended to assist the insertion/positioning of a diagnostic/therapeutic device(s) [e.g., endoscope, catheter] within the gastrointestinal (GI) and/or urinary tract. It is typically coated with a plastic material [e.g., polytetrafluoroethylene (PTFE), commonly known as Teflon, or polyethylene (PE)]. It may have radiopaque graduated markings at the distal end to assist in the fluoroscopic monitoring of its advancement/position within the body. This is a single-use device.
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Where to buy WallStent
We do not have contact details for Lake Region Medical Limited yet. Send a request and we will route it to the right person for your country.
WallStent 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 |
|---|---|---|---|
| MDTBG-023V | — | Not stated | Available |
Procedures that use guidewires
Frequently asked questions
What is WallStent used for?
A metal coil or wire intended to assist the insertion/positioning of a diagnostic/therapeutic device(s) [e.g., endoscope, catheter] within the gastrointestinal (GI) and/or urinary tract. It is typically coated with a plastic material [e.g., polytetrafluoroethylene (PTFE), commonly known as Teflon, or polyethylene (PE)]. It may have radiopaque graduated markings at the distal end to assist in the fluoroscopic monitoring of its advancement/position within the body. This is a single-use device.
Who makes WallStent?
WallStent is made by Lake Region Medical Limited. It is listed under guidewires in our device library.
What sizes does WallStent come in?
The FDA device database does not list sizes for WallStent. Check the instructions for use or ask a Lake Region Medical Limited representative.
Is WallStent MRI safe?
The FDA device database entry for WallStent does not state its MRI safety status. Check the labeling before MRI.
Is WallStent FDA cleared?
WallStent is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Lake Region Medical Limited sales representative?
Lake Region Medical Limited has not listed representatives on LA Vascular yet. Visit the Lake Region Medical Limited 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.