AirView system requirements. Additional Software. Are necessary to download card data, view exported data and reports from AirView. ResMed’s ApneaLink™ Air provides performance and reliability in our most compact, lightweight and easy-to-use home sleep testing device ever. ResMed’s ApneaLink Air is a home sleep testing device that offers advanced features like compatibility with our EasyCare Online patient management tool.

General Information 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. Website: Description: ResMed ApneaLink hardware devices are sleep testing diagnostic products that offers patients the option of having a sleep test at home. The devices record respiratory effort, pulse, oxygen saturation and nasal flow, and reports apneas, hypopneas, flow limitation, snoring, blood oxygen saturation and the probability of Cheyne-Stokes respiration (CSR) breathing patterns.

The ApneaLink Air Software provides clinicians access to a more in-depth view of patients` recordings. This technology uses a proprietary database that saves files on the local computer. Note: There is not a dedicated website for this product but the product download can be found at the bottom of each ApneaLink hardware device page. 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: Section 508 does not apply. This product is considered Medical Technology as defined by the VA in the Medical Device Isolation Architecture (MDIA). For additional information or assistance regarding Section 508, please contact the Section 508 Office at Section508@va.gov.

Download Essentials Of Electronics Petruzella Pdf Files. Decision: Decision Constraints: Per the May 5th, 2015 memorandum from the VA Chief Information Security Officer (CISO) FIPS 140-2 Validate Full Disk Encryption (FOE) for Data at Rest in Database Management Systems (DBMS) and in accordance with Federal requirements and VA policy, database management must use Federal Information Processing Standards (FIPS) 140-2 compliant encryption to protect the confidentiality and integrity of VA information at rest at the application level. If FIPS 140-2 encryption at the application level is not technically possible, FIPS 140-2 compliant full disk encryption (FOE) must be implemented on the hard drive where the DBMS resides. Appropriate access enforcement and physical security control must also be implemented. All instances of deployment using this technology should be reviewed to ensure compliance with and It is the responsibility of the system owner to work with the local CIO (or designee) and Information Security Officer (ISO) to ensure that a compliant DBMS technology is selected and that if needed, mitigating controls are in place and documented in a System Security Plan (SSP).