Biopsy needles
Lee Medical
by Tarca LLC
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.
Lee Medical models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| B-114 | — | Not stated | Available |
| B-115 | — | Not stated | Available |
| B-133 | — | Not stated | Available |
| TP-114 | — | Not stated | Available |
| TP-115 | — | Not stated | Available |
| TP-133 | — | Not stated | Available |
Procedures that use biopsy needles
Frequently asked questions
What is Lee Medical 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 Lee Medical?
Lee Medical is made by Tarca LLC. It is listed under biopsy needles and systems in our device library.
What sizes does Lee Medical come in?
The FDA device database does not list sizes for Lee Medical. Check the instructions for use or ask a Tarca LLC representative.
Is Lee Medical MRI safe?
The FDA device database entry for Lee Medical does not state its MRI safety status. Check the labeling before MRI.
Is Lee Medical FDA cleared?
Lee Medical is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Tarca LLC sales representative?
Tarca LLC has not listed representatives on LA Vascular yet. Visit the Tarca 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.