Examples of Sealed Source and Device Registry in a sentence
A licensee shall use only sealed sources for diagnostic medical uses as approved in the Sealed Source and Device Registry.
Each device has been registered in the Sealed Source and Device Registry.
Note: The NRC maintains the National Sealed Source and Device Registry (NSSDR).
Before adding to or changing the address or addresses of use identified in the application or on the license; and(7) Before it receives a sealed source from a different manufacturer or of a different model number than authorized by its license unless the sealed source is used for manual brachytherapy, is listed in the Sealed Source and Device Registry, and is in a quantity and for an isotope authorized by the license.
The final rule eliminates the references to a sealed source of cobalt-60 or cesium-137 and specifies instead that a licensee shall use sealed sources in photon emitting remote afterloader units, teletherapy units, or gamma stereotactic radiosurgery units: (1) as approved in the Sealed Source and Device Registry; or (2) in research in accordance with an effective Investigational Device Exemption (IDE) application accepted by the FDA provided the requirements of § 35.49(a) are met.
The manual brachytherapy sources may be used for manual brachytherapy uses that are not explicitly listed in the Sealed Source and Device Registry but must be used in accordance with the radiation safety conditions and limitations described in the Sealed Source and Device Registry; orb.
Any planning related queries should be directed to the Local Planning Authority: Reading Borough Council Telephone: 0118 937 3787 Civic Offices Web: www.
Any licensee who possesses sealed sources shall have each sealed source containing radioactive material [, other than hydrogen 3, with a half-life greater than 30 days inany form other than gas] tested for leakage at intervals not to exceed 6 months, unless a longer interval is authorized by the Division [.] , the Nuclear Regulatory Commission or an agreement state in the Sealed Source and Device Registry maintained by the Nuclear Regulatory Commission.
As approved in the Sealed Source and Device Registry for manual brachytherapy medical use.
The final rule, in § 35.500, eliminates the listing of permissible sealed sources and specifies that a licensee may use only sealed sources for diagnostic medical uses as approved in the Sealed Source and Device Registry.