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VA Technical Reference Model v 24.4

Genie Medical
Genie Medical Technology

General InformationGeneral Information help

Technologies must be operated and maintained in accordance with Federal and Department security and privacy policies and guidelines. More information on the proper use of the TRM can be found on the TRM Proper Use Tab/Section.

Website: Go to site
Description: The Genie Medical software programs the Ponto bone anchored hearing aid, ConnectClip, and Oticon Opn (Open) hearing aid processors. This technology allows the audiologist to program the output of these devices according to the individual`s hearing loss with in-situ audiometry. Genie Medical provides a pediatric fitting mode that provides professionals a centralized way to view and change children`s hearing aid settings.

This technology can use a proprietary Genie Medical BAHS (BrainHearing) database to store data. This method is optional and is not included in all editions; users may also store data on local storage devices if necessary.

Genie Medical differs from the Genie and Genie 2 software, which is also produced by the vendor.

This technology is available in multiple editions that the vendor dictates with versioning. These editions provide proprietary functionality for different releases of the vendor`s associated hardware.

Please note that there is no specific product page for this technology and thus the webpage for the hearing device this software supports is used in its place (Ponto hearing aid).

This technology does not use a database to store data.
Technology/Standard Usage Requirements: Users must ensure their use of this technology/standard is consistent with VA policies and standards, including, but not limited to, VA Handbooks 6102 and 6500; VA Directives 6004, 6513, and 6517; and National Institute of Standards and Technology (NIST) standards, including Federal Information Processing Standards (FIPS). Users must ensure sensitive data is properly protected in compliance with all VA regulations. Prior to use of this technology, users should check with their supervisor, Information Security Officer (ISO), Facility Chief Information Officer (CIO), or local Office of Information and Technology (OI&T) representative to ensure that all actions are consistent with current VA policies and procedures prior to implementation.
Section 508 Information: This technology has been assessed by the Section 508 Office and found non-conformant. The Implementer of this technology has the responsibility to ensure the version deployed is 508-compliant. Section 508 compliance may be reviewed by the Section 508 Office and appropriate remedial action required if necessary. For additional information or assistance regarding Section 508, please contact the Section 508 Office at Please see reference tab for more information concerning product versions.
Decision: View Decisions

Decision Source: TRM Mgmt Group
Decision Process: One-VA TRM v23.10
Decision Date: 10/28/2023 at 03:30:53 UTC
Introduced By: TRM Request
Vendor Name: Oticon Medical
- The information contained on this page is accurate as of the Decision Date (10/28/2023 at 03:30:53 UTC).