Biopsy needles
Invivo
by Philips Ds North America LLC
A sterile, sharp bevel-edged, hollow tubular metal instrument designed to remove fluid from a body cavity or to obtain a biopsy specimen from a patient through aspiration; it is not dedicated to a particular part of the anatomy. The device is typically longer than a hypodermic needle and usually has a wider hub. It is not intended for administration of pharmaceuticals. This is a single-use device.
Invivo 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 |
|---|---|---|---|
| 98960320276 | Needle Gauge 20 G; Length 100 mm | MR Conditional | Available |
Procedures that use biopsy needles
Frequently asked questions
What is Invivo used for?
A sterile, sharp bevel-edged, hollow tubular metal instrument designed to remove fluid from a body cavity or to obtain a biopsy specimen from a patient through aspiration; it is not dedicated to a particular part of the anatomy. The device is typically longer than a hypodermic needle and usually has a wider hub. It is not intended for administration of pharmaceuticals. This is a single-use device.
Who makes Invivo?
Invivo is made by Philips Ds North America LLC. It is listed under biopsy needles and systems in our device library.
What sizes does Invivo come in?
Sizes listed for Invivo: Needle Gauge: 20 G; Length: 100 mm. Confirm availability with the manufacturer's instructions for use.
Is Invivo MRI safe?
The FDA device database lists Invivo as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Invivo FDA cleared?
Invivo is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Philips Ds North America LLC sales representative?
Philips Ds North America LLC has not listed representatives on LA Vascular yet. Visit the Philips Ds North America 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.