Biopsy needles
BEXCORE Breast Biopsy System
An assembly of devices intended to be used in conjunction with mammography to insert biopsy devices, typically designated needles, into a breast in order to extract a biopsy of a suspect tumour for diagnostic purposes. It consists of a biopsy unit with needle guides, needles, an examination table, and an integral computer for communicating lesion coordinates. This GMDN code includes stand-alone units as well as units that mount onto an existing mammographic radiographic unit.
BEXCORE Breast Biopsy System 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 |
|---|---|---|---|
| Bexcore System-BXS100 | — | Not stated | Available |
| BXS100 | — | Not stated | Available |
Procedures that use biopsy needles
Frequently asked questions
What is BEXCORE Breast Biopsy System used for?
An assembly of devices intended to be used in conjunction with mammography to insert biopsy devices, typically designated needles, into a breast in order to extract a biopsy of a suspect tumour for diagnostic purposes. It consists of a biopsy unit with needle guides, needles, an examination table, and an integral computer for communicating lesion coordinates. This GMDN code includes stand-alone units as well as units that mount onto an existing mammographic radiographic unit.
Who makes BEXCORE Breast Biopsy System?
BEXCORE Breast Biopsy System is made by MedicalPark CO.,LTD.. It is listed under biopsy needles and systems in our device library.
What sizes does BEXCORE Breast Biopsy System come in?
The FDA device database does not list sizes for BEXCORE Breast Biopsy System. Check the instructions for use or ask a MedicalPark CO.,LTD. representative.
Is BEXCORE Breast Biopsy System MRI safe?
The FDA device database entry for BEXCORE Breast Biopsy System does not state its MRI safety status. Check the labeling before MRI.
Is BEXCORE Breast Biopsy System FDA cleared?
BEXCORE Breast Biopsy System is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a MedicalPark CO.,LTD. sales representative?
MedicalPark CO.,LTD. has not listed representatives on LA Vascular yet. Visit the MedicalPark CO.,LTD. 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.