Biopsy needles

Cassi

by Scion Medical Techologies, LLC

A sterile, sharp bevel-edged, hollow tubular metal instrument designed to percutaneously obtain a specimen of soft tissue, typically for histopathological examination. The device is usually attached to a syringe for the aspiration of the specimen; it is available in a variety of lengths, diameters (bores), and tip configurations (e.g., straight or curved). This is a single-use device.

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Cassi models and sizes

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

Model / catalog no.SizeMRIStatus
CS-2001-CC-10Length 2 cm Not statedAvailable
CS2001-BHLength 2 cm Not statedAvailable
CS2100-NT-1Length 2 cm Not statedAvailable
CS2120-NT-1Length 2 cm Not statedAvailable

Procedures that use biopsy needles

Frequently asked questions

What is Cassi used for?

A sterile, sharp bevel-edged, hollow tubular metal instrument designed to percutaneously obtain a specimen of soft tissue, typically for histopathological examination. The device is usually attached to a syringe for the aspiration of the specimen; it is available in a variety of lengths, diameters (bores), and tip configurations (e.g., straight or curved). This is a single-use device.

Who makes Cassi?

Cassi is made by Scion Medical Techologies, LLC. It is listed under biopsy needles and systems in our device library.

What sizes does Cassi come in?

Sizes listed for Cassi: Length: 2 cm. Confirm availability with the manufacturer's instructions for use.

Is Cassi MRI safe?

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

Is Cassi FDA cleared?

Cassi is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Scion Medical Techologies, LLC sales representative?

Scion Medical Techologies, LLC has not listed representatives on LA Vascular yet. Visit the Scion Medical Techologies, 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.

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