Infusion catheters
SclereSafe
A flexible dual-lumen tube designed to be percutaneously introduced into an insufficient vein [commonly the greater saphenous vein (GSV)] to inject sclerosing solution and simultaneously aspirate blood, to shrink and close the varicose vein as part of an endovenous chemical ablation procedure. It is intended to be used with a dedicated injection/aspiration syringe which may be provided with the catheter. This is a single-use device.
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Where to buy SclereSafe
Contact V.v.t. Med Ltd directly; they can quote, ship, or point you to the distributor for your country.
From vvtmed.com, checked November 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
SclereSafe 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 |
|---|---|---|---|
| 150 | — | Not stated | Available |
FDA clearances
- 510(k) K231148 June 2023
Procedures that use infusion catheters
Frequently asked questions
What is SclereSafe used for?
A flexible dual-lumen tube designed to be percutaneously introduced into an insufficient vein [commonly the greater saphenous vein (GSV)] to inject sclerosing solution and simultaneously aspirate blood, to shrink and close the varicose vein as part of an endovenous chemical ablation procedure. It is intended to be used with a dedicated injection/aspiration syringe which may be provided with the catheter. This is a single-use device.
Who makes SclereSafe?
SclereSafe is made by V.v.t. Med Ltd. It is listed under thrombolysis infusion catheters in our device library.
What sizes does SclereSafe come in?
The FDA device database does not list sizes for SclereSafe. Check the instructions for use or ask a V.v.t. Med Ltd representative.
Is SclereSafe MRI safe?
The FDA device database entry for SclereSafe does not state its MRI safety status. Check the labeling before MRI.
Is SclereSafe FDA cleared?
SclereSafe is covered by FDA submission K231148.
How do I contact a V.v.t. Med Ltd sales representative?
V.v.t. Med Ltd has not listed representatives on LA Vascular yet. Visit the V.v.t. Med Ltd 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.