Y-90 microspheres
TheraSphere Administration Set
A device that is a naturally-occurring, accelerator- or reactor-produced radioactive isotope and intended to be permanently implanted into the body in order to deliver curative or palliative radiotherapy treatments. It is typically placed in the body by means of an applicator using either fluoroscopic or endoscopic guidance. Manually implanted sources intended for permanent implantation are designed to be histocompatible. It may take the form of, e.g., microspheres, spheres, stents, seeds or wires selected for producing low energy photons, beta or alpha particles.
TheraSphere Administration Set 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 |
|---|---|---|---|
| 990226.SPE | — | Not stated | Available |
| OTT-SPE-FP-001 | — | Not stated | Available |
Procedures that use y-90 microspheres
Frequently asked questions
What is TheraSphere Administration Set used for?
A device that is a naturally-occurring, accelerator- or reactor-produced radioactive isotope and intended to be permanently implanted into the body in order to deliver curative or palliative radiotherapy treatments. It is typically placed in the body by means of an applicator using either fluoroscopic or endoscopic guidance. Manually implanted sources intended for permanent implantation are designed to be histocompatible. It may take the form of, e.g., microspheres, spheres, stents, seeds or wires selected for producing low energy photons, beta or alpha particles.
Who makes TheraSphere Administration Set?
TheraSphere Administration Set is made by Biocompatibles Uk Ltd. It is listed under y-90 radioembolization microspheres in our device library.
What sizes does TheraSphere Administration Set come in?
The FDA device database does not list sizes for TheraSphere Administration Set. Check the instructions for use or ask a Biocompatibles Uk Ltd representative.
Is TheraSphere Administration Set MRI safe?
The FDA device database entry for TheraSphere Administration Set does not state its MRI safety status. Check the labeling before MRI.
Is TheraSphere Administration Set FDA cleared?
TheraSphere Administration Set is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Biocompatibles Uk Ltd sales representative?
Biocompatibles Uk Ltd has not listed representatives on LA Vascular yet. Visit the Biocompatibles Uk 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.