RADIOACTIVE MATERIAL LICENSE
Forms and Information
General License Registration
Note on Return of Devices and Receipt of New Devices
When a general license device is returned to the manufacturer or other specific licensee authorized to receive such device, you are required to report this transfer to MDE by using the Transfer Declaration Form
, in accordance with COMAR 26.12.01.01C.22(d)(4)(viii). The transferred device will be removed from the Department's database. If you obtain additional or replacement devices, you are required to report these new devices to the Department within 30 days of receipt by submitting a new General License Device Registration Form.
The new devices will be added to the Department's database. These notifications are necessary for MDE to maintain current information on general license devices in Maryland.
Note on Annual Registration Update
An annual update of registration information is required, in accordance with COMAR 26.12.01.01C.22(k)(1). Instructions for this update will be provided with your annual invoice. If you have any questions about this annual update, please e-mail your inquiry to MDE.GENLIC@maryland.gov
or call Mr. Atnatiwos Meshesha at 410-537-3300.
Note on High Dose-Rate Brachytherapy Remote Afterloader - 2021
The use of HDR remote afterloaders for patient treatements using sources above 10 Curies
shall be approved by the U.S. Food and Drug Administration and U.S. Nuclear Regulatory Commission. All applicable licensees please check the following Memo below in the link and the note from US NRC. For more information you can contact Mr. Atnatiwos Meshesha at firstname.lastname@example.org or call Ms. Cheryl Nitkowski or Mr. Atnatiwos Meshesha at 410-537-3300.
For information on licensing of radioactive materials. on reciprocity, or on general licensing, please contact Atnatiwos Meshesha at email@example.com. Mr. Meshesha may be reached at