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Radionuclide Teletherapy Source Suppliers

 EMAIL INQUIRY to  3 suppliers  
Philips Medical Systems, N.A. | Address: 22100 Bothell Everett Highway PO Box 3003, Bothell, Washington 98041-3003, USA USA
www.medical.philips.com/us | Phone: +1-(425)-487-7000, 800-934-7372
FDA Registration: 1218950  Annual Revenues: > USD 1 Billion  Employee Count: ~35550
Products: Defibrillators, Defibrillator Testers (FDA Code: DRL), Electrocardiographs (ECGs), CT / MRI Based, CT Scanners, Automated External Defibrillators (AEDs), ...
Philips Medical Systems, N.A. manufactures systems for imaging, radiation oncology & patient monitoring, as well as renders information management & resuscitation products. Our heartstart home defibri more...
 
International Isotopes Idaho, Inc. | Address: 4137 Commerce Circle, Idaho Falls, Idaho 83401, USA USA
www.intisoid.com | Phone: +1-(208)-524-5300, 800-699-3108
FDA Registration: 3034521
Products: Nuclear Flood Source Phantom (FDA Code: IYQ), Nuclear Sealed Calibration Source (FDA Code: IXD), Radionuclide Teletherapy Source (FDA Code: IWH), ...
International Isotopes Idaho, Inc. develops & deploys technological solutions for a variety of applications, including cancer treatment, nuclear pharmacy, medical diagnostics and medical therapy produ more...
Neutron Products Inc | Address: 22301 Mt. Ephraim Road, Box 68, Dickerson, Maryland 20842, USA USA
Send Inquiry | Phone: +1-(301)-349-5001, 800-424-8169
Year Established: 1959  Annual Revenues: USD 5-10 Million  Employee Count: ~50
Products: Radiation Sterilizer, Radionuclide Teletherapy Source (FDA Code: IWH), Therapeutic X-Ray Beam Limiting Device (FDA Code: KQA), ...
Neutron Products Inc specializes in offering radiation sterilizers and radionuclide teletherapy sources. more...
 EMAIL INQUIRY to  3 Radionuclide Teletherapy Source suppliers  
FDA Code / Regulation: IWH / 892.5740

A radionuclide teletherapy source is a device consisting of a radionuclide enclosed in a sealed container. The device is intended for radiation therapy, with the radiation source located at a distance from the patient's body.

Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 892.9.

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