Neuro aspiration catheters

Raptor Aspiration Catheter

by Balt USA LLC

A flexible or semi-flexible tube designed for the percutaneous, transluminal disruption and removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction in native/stented blood vessels, native/synthetic bypass grafts, and/or haemodialysis access grafts, through suction (aspiration) in conjunction with a syringe or dedicated suction pump system (pump not included). It may additionally be intended for infusion of fluids and/or used as a guide-catheter to facilitate introduction of a thrombectomy wire-net (not included) to remove residual thrombus. Collection containers may be included with the catheter. This is a single-use device.

Ask about this device Where to buy Compare similar devices

Where to buy Raptor Aspiration Catheter

We do not have contact details for Balt USA LLC yet. Send a request and we will route it to the right person for your country.

Request this device

Is this your product? Claim Balt USA LLC to list your reps and distributors by country and receive buyer requests from your territories.

Raptor Aspiration Catheter models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
RPTR038145β€” Not statedAvailable
RPTR038155β€” Not statedAvailable
RPTR038160β€” Not statedAvailable
RPTR054125β€” Not statedAvailable
RPTR054135β€” Not statedAvailable
RPTR054145β€” Not statedAvailable
RPTR054150β€” Not statedAvailable
RPTR071128Length 128 cm; Outer Diameter 0.083 in; Catheter Inner Diameter 0.071 in Not statedAvailable
RPTR071132Catheter Inner Diameter 0.071 in; Outer Diameter 0.083 in; Length 132 cm Not statedAvailable
RPTR071140β€” Not statedAvailable
RPTR074120Length 120 cm; Outer Diameter 0.086 in; Catheter Inner Diameter 0.074 in Not statedAvailable
RPTR074132Outer Diameter 0.086 in; Length 132 cm; Catheter Inner Diameter 0.074 in Not statedAvailable
RPTR074140β€” Not statedAvailable

FDA clearances

  • 510(k) K243948 June 2025
  • 510(k) K234083 July 2024

Procedures that use neuro aspiration catheters

Frequently asked questions

What is Raptor Aspiration Catheter used for?

A flexible or semi-flexible tube designed for the percutaneous, transluminal disruption and removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction in native/stented blood vessels, native/synthetic bypass grafts, and/or haemodialysis access grafts, through suction (aspiration) in conjunction with a syringe or dedicated suction pump system (pump not included). It may additionally be intended for infusion of fluids and/or used as a guide-catheter to facilitate introduction of a thrombectomy wire-net (not included) to remove residual thrombus. Collection containers may be included with the catheter. This is a single-use device.

Who makes Raptor Aspiration Catheter?

Raptor Aspiration Catheter is made by Balt USA LLC. It is listed under neurovascular aspiration catheters in our device library.

What sizes does Raptor Aspiration Catheter come in?

Sizes listed for Raptor Aspiration Catheter: Length: 120–132 cm; Outer Diameter: 0.08–0.09 in; Catheter Inner Diameter: 0.07–0.07 in. Confirm availability with the manufacturer's instructions for use.

Is Raptor Aspiration Catheter MRI safe?

The FDA device database entry for Raptor Aspiration Catheter does not state its MRI safety status. Check the labeling before MRI.

Is Raptor Aspiration Catheter FDA cleared?

Raptor Aspiration Catheter is covered by FDA submissions K234083, K243948.

How do I contact a Balt USA LLC sales representative?

Balt USA LLC has not listed representatives on LA Vascular yet. Visit the Balt USA LLC 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.

πŸ“¬ The IR Device Brief

One email a month: new FDA clearances, recalls and device pages in vascular & interventional radiology.

We'll email you a link to confirm. Unsubscribe any time.

Suggest edits

For manufacturers and their teams. Each field shows what the page says now: add, remove or rewrite anything, and leave the rest as is. LA Vascular reviews every change before it goes live.

About you