Biopsy needles

Bone biopsy cannula

by Möller Medical GmbH

A sterile, sharp bevel-edged, hollow tubular metal instrument designed to obtain a specimen of bone, bone marrow and/or tumour from any bone of the body. It is typically inserted through a bone access cannula under imaging [e.g., fluoroscopic, ultrasonic, computed tomography (CT)] control and supplied with an ejector rod to remove the biopsy. This is a single-use device.

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Bone biopsy cannula models and sizes

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

Model / catalog no.SizeMRIStatus
BOY-1080-16-0075— Not statedAvailable
BOY-1080-16-0125— Not statedAvailable
BOY-1080-16-0165— Not statedAvailable

Procedures that use biopsy needles

Frequently asked questions

What is Bone biopsy cannula used for?

A sterile, sharp bevel-edged, hollow tubular metal instrument designed to obtain a specimen of bone, bone marrow and/or tumour from any bone of the body. It is typically inserted through a bone access cannula under imaging [e.g., fluoroscopic, ultrasonic, computed tomography (CT)] control and supplied with an ejector rod to remove the biopsy. This is a single-use device.

Who makes Bone biopsy cannula?

Bone biopsy cannula is made by Möller Medical GmbH. It is listed under biopsy needles and systems in our device library.

What sizes does Bone biopsy cannula come in?

The FDA device database does not list sizes for Bone biopsy cannula. Check the instructions for use or ask a Möller Medical GmbH representative.

Is Bone biopsy cannula MRI safe?

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

Is Bone biopsy cannula FDA cleared?

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

How do I contact a Möller Medical GmbH sales representative?

Möller Medical GmbH has not listed representatives on LA Vascular yet. Visit the Möller Medical GmbH 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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