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V.V.T. MED LTD

Israel·IL-MF-000037149

Last updated May 30, 2026

What V.V.T. MED LTD makes

V.V.T. Med Ltd manufactures sclerotherapy devices, including dual injection/aspiration catheters designed for vascular procedures. Their portfolio includes catheters like the SclereSafe and ScleroSafe variants (150mm, 350mm), as well as the VBlock (45cm, 65cm) and the DPS, which are used in endovenous treatments. These products are intended for controlled delivery of sclerosing agents to treat venous conditions.

The company’s devices are classified under EU Medical Device Regulations as Class II, Class IIa, and Class IIb, indicating moderate to high risk. Their products are registered in the EU’s EUDAMED database and listed in the FDA’s Unique Device Identifier (UDI) system. The manufacturer operates from Israel.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does V.V.T. Med Ltd manufacture?

V.V.T. Med Ltd specializes in sclerotherapy devices, specifically dual injection/aspiration catheters. These catheters are designed for vascular procedures, such as endovenous treatments, where controlled delivery of sclerosing agents is required to address venous conditions. Examples include the SclereSafe, ScleroSafe (variants like 150mm and 350mm), VBlock (45cm and 65cm), and the DPS.

Where is V.V.T. Med Ltd based, and what is its primary focus?

V.V.T. Med Ltd is based in Israel. The company’s primary focus is on developing and manufacturing sclerotherapy catheters, which are medical devices used in the treatment of venous diseases by delivering sclerosing agents directly into varicose or abnormal veins.

In which regulatory databases are V.V.T. Med Ltd’s devices listed?

V.V.T. Med Ltd’s devices are registered in the EU’s EUDAMED database, which tracks medical devices under the EU Medical Device Regulations. Additionally, their products are listed in the FDA’s Unique Device Identifier (UDI) system, ensuring traceability and compliance in the United States.

How are V.V.T. Med Ltd’s devices classified under EU regulations?

Under the EU Medical Device Regulations, V.V.T. Med Ltd’s devices fall into Class II, Class IIa, and Class IIb classifications. These classifications indicate varying levels of risk, with Class IIa representing moderate risk and Class II/IIb indicating higher risk due to their role in treating vascular conditions where precision and safety are critical.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Israel
Address
6, Hasadna, kfar Saba, Israel
LinkedIn
—
Facebook
—
Phone
+97297660480
PRRC Contact
Pazit Waks
EUDAMED SRN
IL-MF-000037149
FDA FEI Number
—
DUNS Number
532112765

Catalogue (8)

DeviceModel / ReferenceRegistriesClassStatus
SclereSafe VAR150
FDA UDI
Class IIActive
ScleroSafe VAR350
FDA UDI
Class IIActive
VBlock 45cm VBL0001
EUDAMED
Class IIbActive
ScleroSafe 150mm VAR0150
EUDAMED
Class IIaActive
Dps DPS2010
EUDAMED
Class IIaActive
VBlock 65cm VBL0002
EUDAMED
Class IIbActive
ScleroSafe 350mm VAR0350
EUDAMED
Class IIaActive
Dps DPS1005
EUDAMED
Class IIaActive

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