Y-90 microspheres
TheraSphere Administration Accessory Kit (US)
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 Accessory Kit (US) 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 |
|---|---|---|---|
| K125914-001 | — | Not stated | Available |
Procedures that use y-90 microspheres
Frequently asked questions
What is TheraSphere Administration Accessory Kit (US) 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 Accessory Kit (US)?
TheraSphere Administration Accessory Kit (US) is made by Biocompatibles Uk Ltd. It is listed under y-90 radioembolization microspheres in our device library.
What sizes does TheraSphere Administration Accessory Kit (US) come in?
The FDA device database does not list sizes for TheraSphere Administration Accessory Kit (US). Check the instructions for use or ask a Biocompatibles Uk Ltd representative.
Is TheraSphere Administration Accessory Kit (US) MRI safe?
The FDA device database entry for TheraSphere Administration Accessory Kit (US) does not state its MRI safety status. Check the labeling before MRI.
Is TheraSphere Administration Accessory Kit (US) FDA cleared?
TheraSphere Administration Accessory Kit (US) 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.