Embolic beads

QuadraSphere

by BioSphere Medical

A non-bioabsorbable, implantable bead/microsphere intended to be introduced into the peripheral vasculature during an interventional radiology procedure to treat hypervascularized tumours and arteriovenous malformation in a variety of anatomies (e.g., head, neck, spine, liver, genitourinary tract, uterus, gastrointestinal, limbs and lungs); it does not include a pharmaceutical agent. It is typically available as injectable solution containing numerous microspheres [e.g., compressible polyvinyl alcohol (PVA) microspheres] intended to permanently obstruct blood flow to the tumour/malformation.

Contact a rep Compare similar devices

QuadraSphere models and sizes

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

Model / catalog no.SizeMRIStatus
00884450106099β€” Not statedAvailable
00884450113875β€” Not statedAvailable
00884450118467β€” Not statedAvailable
00884450118948β€” Not statedAvailable
00884450275160β€” Not statedAvailable
00884450275177β€” Not statedAvailable
00884450275184β€” Not statedAvailable
00884450275191β€” Not statedAvailable

Procedures that use embolic beads

Frequently asked questions

What is QuadraSphere used for?

A non-bioabsorbable, implantable bead/microsphere intended to be introduced into the peripheral vasculature during an interventional radiology procedure to treat hypervascularized tumours and arteriovenous malformation in a variety of anatomies (e.g., head, neck, spine, liver, genitourinary tract, uterus, gastrointestinal, limbs and lungs); it does not include a pharmaceutical agent. It is typically available as injectable solution containing numerous microspheres [e.g., compressible polyvinyl alcohol (PVA) microspheres] intended to permanently obstruct blood flow to the tumour/malformation.

Who makes QuadraSphere?

QuadraSphere is made by BioSphere Medical. It is listed under embolic microspheres and particles (beads) in our device library.

What sizes does QuadraSphere come in?

The FDA device database does not list sizes for QuadraSphere. Check the instructions for use or ask a BioSphere Medical representative.

Is QuadraSphere MRI safe?

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

Is QuadraSphere FDA cleared?

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

How do I contact a BioSphere Medical sales representative?

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

πŸ“¬ The IR Device Brief

One email a month: new FDA clearances, recalls and device pages in vascular & interventional radiology.

We'll email you a link to confirm. Unsubscribe any time.

Suggest edits

For manufacturers and their teams. Each field shows what the page says now: add, remove or rewrite anything, and leave the rest as is. LA Vascular reviews every change before it goes live.

About you