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Venous Stents & Pulmonary EmbolismApril 4, 2021INVAMED Medical Affairs

MultiBEAM IVC Filter: Design & Indications Overview

MultiBEAM IVC filter by INVAMED: a retrievable inferior vena cava filter designed to reduce PE risk when anticoagulation is contraindicated. See design.

The MultiBEAM Inferior Vena Cava (IVC) Filter is a convertible or retrievable filter manufactured by INVAMED, designed to intercept thromboembolic material traveling through the inferior vena cava and reduce the risk of pulmonary embolism (PE) in appropriately selected patients. This overview summarizes the device's design, mechanism, and indication concepts for clinicians evaluating IVC filter options.

What Is the MultiBEAM IVC Filter?

MultiBEAM is designed to capture and retain thromboembolic fragments traveling within the venous system from the lower extremities or pelvis, reducing the likelihood that they reach the pulmonary circulation. The device features a self-expanding metallic framework intended to provide stable fixation within the IVC while maintaining vessel patency and venous return.

Device availability and regulatory status vary by country. Please contact INVAMED or your authorized local distributor for current regulatory information applicable to your region.

What Is the Design of the MultiBEAM Filter?

Key design elements include:

  • Self-expanding nitinol struts — engineered from a biocompatible alloy for secure anchoring under variable venous pressures
  • Multi-spoke ("beam") configuration — creates multiple capture zones intended to trap emboli efficiently without significantly restricting blood flow
  • Retrievable or optionally permanent configurations — certain models allow retrieval within a designated timeframe, while others are intended to function as permanent PE prophylaxis, offering clinicians flexibility based on the clinical scenario
  • Migration and tilt resistance — struts are designed to be precisely balanced to help reduce filter migration or tilting over time

What Is the Deployment Approach?

MultiBEAM is deployed using an over-the-wire or sheath-based technique, typically via femoral or jugular venous access, under fluoroscopic guidance. As with all endovascular filter placements, precise positioning within the IVC is confirmed with imaging before the delivery system is withdrawn.

What Are the Indication Concepts for IVC Filters?

IVC filters, including MultiBEAM, are generally considered in patients with venous thromboembolism (VTE) who have:

  • A contraindication to anticoagulation therapy (for example, active bleeding or a recent major surgery)
  • An inadequate response to anticoagulation despite appropriate therapy
  • A temporary, time-limited need for mechanical PE prophylaxis while an anticoagulation contraindication is expected to resolve

Contraindications to consider include an excessively narrow or tortuous IVC that prevents secure filter seating, active infection at the intended insertion site, and other patient-specific anatomical constraints. Patient selection for IVC filter placement is determined by the treating physician based on a comprehensive risk assessment.

Why Does Retrieval Matter?

For retrievable configurations, timely retrieval once the anticoagulation contraindication has resolved is an important part of the clinical pathway, as long-term filter dwell time is associated with device-related considerations that clinicians weigh against the ongoing risk of VTE. Institutions often use structured tracking systems to flag retrievable filters for follow-up evaluation and removal planning.

Frequently Asked Questions

When is the MultiBEAM IVC filter typically considered?

It is typically considered for patients with VTE who cannot receive anticoagulation, who have failed anticoagulation therapy, or who need temporary mechanical PE prophylaxis. The decision is individualized and made by the treating physician.

What is the difference between a retrievable and permanent configuration?

Retrievable configurations are designed to be removed within a defined window once the clinical need has passed, while permanent configurations remain in place indefinitely as ongoing PE prophylaxis. The appropriate choice depends on the anticipated duration of the anticoagulation contraindication.

Where can clinicians find complete technical specifications?

Complete technical specifications, sizing information, and the official Instructions for Use (IFU) are available through INVAMED or by contacting INVAMED directly for product documentation.

Related INVAMED Resources


Medical Disclaimer: This article is provided for general informational and educational purposes only and does not constitute medical advice, diagnosis, or treatment recommendation. It is not a substitute for consultation with a qualified healthcare professional. Product indications, availability, and regulatory status vary by country. Always refer to the official Instructions for Use (IFU) and consult a licensed physician for guidance specific to your situation. INVAMED devices are intended for use by trained healthcare professionals.

Reviewed by: INVAMED Medical Affairs

This content is prepared for educational purposes for healthcare professionals and does not constitute medical advice. Always consult clinical guidelines and product instructions for use.

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