Biopsy needles
NeoNavia Biopsy System
An invasive tubular surgical instrument designed to be connected to a biopsy gun handpiece (not included) for the automatic extraction of a core tissue sample from an anatomical structure (a biopsy), while causing minimal surrounding tissue damage, for tissue pathological examination/testing. It is an open, cylindrical needle intended to be percutaneously inserted, typically under image guidance, and is typically used to obtain samples of soft tissue from the kidneys, prostate, pancreas, liver, and breast. This is a single-use device.
NeoNavia 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 |
|---|---|---|---|
| 1102 | — | MR Unsafe | Available |
| 1103 | — | MR Unsafe | Available |
| 2104 | Needle Gauge 14 G | MR Unsafe | Available |
Procedures that use biopsy needles
Frequently asked questions
What is NeoNavia Biopsy System used for?
An invasive tubular surgical instrument designed to be connected to a biopsy gun handpiece (not included) for the automatic extraction of a core tissue sample from an anatomical structure (a biopsy), while causing minimal surrounding tissue damage, for tissue pathological examination/testing. It is an open, cylindrical needle intended to be percutaneously inserted, typically under image guidance, and is typically used to obtain samples of soft tissue from the kidneys, prostate, pancreas, liver, and breast. This is a single-use device.
Who makes NeoNavia Biopsy System?
NeoNavia Biopsy System is made by NeoDynamics AB (publ). It is listed under biopsy needles and systems in our device library.
What sizes does NeoNavia Biopsy System come in?
Sizes listed for NeoNavia Biopsy System: Needle Gauge: 14 G. Confirm availability with the manufacturer's instructions for use.
Is NeoNavia Biopsy System MRI safe?
The FDA device database lists NeoNavia Biopsy System as MR Unsafe. Always follow the specific MRI conditions in the labeling.
Is NeoNavia Biopsy System FDA cleared?
NeoNavia Biopsy System is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a NeoDynamics AB (publ) sales representative?
NeoDynamics AB (publ) has not listed representatives on LA Vascular yet. Visit the NeoDynamics AB (publ) 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.